Canonical Allele Identifier: CA786938983

Gene: MFSD8

Linked Data

• dbSNP Id: rs1431127671
• gnomAD v3: 4-127939047-G-GA
• gnomAD v4: 4-127939047-G-GA
• MyVariant Identifiers: chr4:g.128860202_128860203insA (hg19) ; chr4:g.127939047_127939048insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127939054dup , CM000666.2:g.127939054dup	GRCh38
NC_000004.11:g.128860209dup , CM000666.1:g.128860209dup	GRCh37
NC_000004.10:g.129079659dup	NCBI36
NG_008657.1:g.31937dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.699-210dup	ENSP00000296468.3:n.699-210dup
ENST00000505284.6:n.915-210dup
ENST00000509826.2:c.698+805dup	ENSP00000421176.2:n.698+805dup
ENST00000513559.6:c.419-212dup	ENSP00000425000.2:n.419-212dup
ENST00000515130.6:c.564-210dup	ENSP00000493056.1:n.564-210dup
ENST00000641025.1:c.699-210dup	ENSP00000493346.1:n.699-210dup
ENST00000641092.1:c.553+2997dup	ENSP00000493392.1:n.553+2997dup
ENST00000641133.1:c.*13-210dup	ENSP00000493192.1:n.*13-210dup
ENST00000641134.1:c.419-210dup	ENSP00000492925.1:n.419-210dup
ENST00000641147.1:c.304+4704dup	ENSP00000493133.1:n.304+4704dup
ENST00000641178.1:c.564-210dup	ENSP00000492989.1:n.564-210dup
ENST00000641186.1:c.585-210dup	ENSP00000493347.1:n.585-210dup
ENST00000641228.1:c.553+2997dup	ENSP00000493194.1:n.553+2997dup
ENST00000641243.1:c.554-210dup	ENSP00000493083.1:n.554-210dup
ENST00000641264.1:c.*496-210dup	ENSP00000492908.1:n.*496-210dup
ENST00000641332.1:c.554-210dup	ENSP00000493397.1:n.554-210dup
ENST00000641340.1:c.698+805dup	ENSP00000493191.1:n.698+805dup
ENST00000641369.1:c.195-210dup	ENSP00000493037.1:n.195-210dup
ENST00000641393.1:c.304+4704dup	ENSP00000493197.1:n.304+4704dup
ENST00000641397.1:c.439+4704dup	ENSP00000493406.1:n.439+4704dup
ENST00000641434.1:c.699-210dup	ENSP00000493279.1:n.699-210dup
ENST00000641464.1:c.449+805dup	ENSP00000493438.1:n.449+805dup
ENST00000641482.1:c.699-210dup	ENSP00000493277.1:n.699-210dup
ENST00000641503.1:c.585-210dup	ENSP00000493304.1:n.585-210dup
ENST00000641508.1:c.698+805dup	ENSP00000493209.1:n.698+805dup
ENST00000641509.1:c.439+4704dup	ENSP00000493459.1:n.439+4704dup
ENST00000641538.1:c.545-210dup
ENST00000641590.1:c.585-210dup	ENSP00000493132.1:n.585-210dup
ENST00000641658.1:c.419-210dup	ENSP00000492987.1:n.419-210dup
ENST00000641686.2:c.699-210dup MANE Select	ENSP00000493218.2:n.699-210dup
ENST00000641690.1:c.553+2997dup	ENSP00000492966.1:n.553+2997dup
ENST00000641695.1:c.699-212dup	ENSP00000493134.1:n.699-212dup
ENST00000641742.1:c.554-210dup	ENSP00000493315.1:n.554-210dup
ENST00000641743.1:c.699-210dup	ENSP00000493130.1:n.699-210dup
ENST00000641748.1:c.699-210dup	ENSP00000493330.1:n.699-210dup
ENST00000641753.1:c.526-210dup
ENST00000641774.1:c.584+805dup	ENSP00000492960.1:n.584+805dup
ENST00000641776.1:c.*251-210dup	ENSP00000493261.1:n.*251-210dup
ENST00000641830.1:c.35-210dup
ENST00000641843.1:c.305-210dup	ENSP00000493174.1:n.305-210dup
ENST00000641869.1:c.4-210dup
ENST00000641870.1:c.554-210dup	ENSP00000493044.1:n.554-210dup
ENST00000641882.1:c.440-210dup	ENSP00000493301.1:n.440-210dup
ENST00000641928.1:c.449+805dup	ENSP00000493418.1:n.449+805dup
ENST00000641949.1:c.553+2997dup	ENSP00000492891.1:n.553+2997dup
ENST00000642012.1:n.353dup
ENST00000642034.1:c.585-210dup	ENSP00000493285.1:n.585-210dup
ENST00000642042.1:c.699-210dup	ENSP00000493260.1:n.699-210dup
ENST00000642078.1:c.419-210dup	ENSP00000492885.1:n.419-210dup
ENST00000642121.1:n.91-8231dup
ENST00000296468.7:c.699-210dup	ENSP00000296468.3:n.699-210dup
ENST00000505284.5:n.594-210dup
ENST00000508441.1:n.566-210dup
ENST00000509826.1:c.449+805dup	ENSP00000421176.1:n.449+805dup
ENST00000513559.5:c.564-210dup	ENSP00000425000.1:n.564-210dup
ENST00000515130.5:n.1145-210dup
NM_152778.2:c.699-210dup	NP_689991.1:n.699-210dup
XM_005262893.1:c.699-210dup	XP_005262950.1:n.699-210dup
XM_005262896.1:c.554-212dup	XP_005262953.1:n.554-212dup
XM_005262897.1:c.553+2997dup	XP_005262954.1:n.553+2997dup
XM_005262898.2:c.699-210dup	XP_005262955.1:n.699-210dup
XM_005262900.2:c.554-210dup	XP_005262957.1:n.554-210dup
XM_011531830.1:c.585-210dup	XP_011530132.1:n.585-210dup
XM_011531831.1:c.439+4704dup	XP_011530133.1:n.439+4704dup
XM_011531832.1:c.585-210dup	XP_011530134.1:n.585-210dup
XR_938717.1:n.776-210dup
NM_001363520.1:c.553+2997dup	NP_001350449.1:n.553+2997dup
NM_001363521.1:c.439+4704dup	NP_001350450.1:n.439+4704dup
XM_005262898.3:c.699-210dup	XP_005262955.1:n.699-210dup
XM_017007989.1:c.553+2997dup	XP_016863478.1:n.553+2997dup
XM_024453981.1:c.564-210dup	XP_024309749.1:n.564-210dup
XM_024453982.1:c.450-210dup	XP_024309750.1:n.450-210dup
XM_024453983.1:c.304+4704dup	XP_024309751.1:n.304+4704dup
XR_001741194.1:n.776-210dup
XR_001741195.1:n.662-210dup
XR_001741196.1:n.630+2997dup
XR_001741197.1:n.631-210dup
XR_001741198.2:n.631-210dup
XR_001741199.1:n.631-210dup
XR_938717.2:n.776-210dup
NM_001363520.2:c.553+2997dup	NP_001350449.1:n.553+2997dup
NM_001363521.2:c.439+4704dup	NP_001350450.1:n.439+4704dup
NM_001371590.1:c.564-210dup	NP_001358519.1:n.564-210dup
NM_001371591.1:c.699-210dup	NP_001358520.1:n.699-210dup
NM_001371592.1:c.705-210dup	NP_001358521.1:n.705-210dup
NM_001371593.1:c.585-210dup	NP_001358522.1:n.585-210dup
NM_001371594.1:c.554-212dup	NP_001358523.1:n.554-212dup
NM_001371595.1:c.419-212dup	NP_001358524.1:n.419-212dup
NM_001371596.2:c.699-210dup MANE Select	NP_001358525.1:n.699-210dup
NM_152778.3:c.699-210dup	NP_689991.1:n.699-210dup
NM_152778.4:c.699-210dup	NP_689991.1:n.699-210dup