Canonical Allele Identifier: CA3077397

Gene: MFSD8

Linked Data

• dbSNP Id: rs199555198
• ExAC: 4:128859948 A / C
• gnomAD v3: 4-127938793-A-C
• gnomAD v4: 4-127938793-A-C
• MyVariant Identifiers: chr4:g.128859948A>C (hg19) ; chr4:g.127938793A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127938793A>C , CM000666.2:g.127938793A>C	GRCh38
NC_000004.11:g.128859948A>C , CM000666.1:g.128859948A>C	GRCh37
NC_000004.10:g.129079398A>C	NCBI36
NG_008657.1:g.32192T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296468.8:c.744T>G	ENSP00000296468.3:p.Asn248Lys
ENST00000505284.6:n.960T>G
ENST00000509826.2:c.698+1060T>G	ENSP00000421176.2:n.698+1060T>G
ENST00000513559.6:c.462T>G	ENSP00000425000.2:p.Asn154Lys
ENST00000515130.6:c.609T>G	ENSP00000493056.1:p.Asn203Lys
ENST00000641025.1:c.744T>G	ENSP00000493346.1:p.Asn248Lys
ENST00000641092.1:c.553+3252T>G	ENSP00000493392.1:n.553+3252T>G
ENST00000641133.1:c.*58T>G	ENSP00000493192.1:n.*58T>G
ENST00000641134.1:c.464T>G	ENSP00000492925.1:p.Ile155Ser
ENST00000641147.1:c.304+4959T>G	ENSP00000493133.1:n.304+4959T>G
ENST00000641178.1:c.609T>G	ENSP00000492989.1:p.Asn203Lys
ENST00000641186.1:c.630T>G	ENSP00000493347.1:p.Asn210Lys
ENST00000641228.1:c.553+3252T>G	ENSP00000493194.1:n.553+3252T>G
ENST00000641243.1:c.599T>G	ENSP00000493083.1:p.Ile200Ser
ENST00000641264.1:c.*541T>G	ENSP00000492908.1:n.*541T>G
ENST00000641332.1:c.599T>G	ENSP00000493397.1:p.Ile200Ser
ENST00000641340.1:c.698+1060T>G	ENSP00000493191.1:n.698+1060T>G
ENST00000641369.1:c.240T>G	ENSP00000493037.1:p.Asn80Lys
ENST00000641393.1:c.304+4959T>G	ENSP00000493197.1:n.304+4959T>G
ENST00000641397.1:c.439+4959T>G	ENSP00000493406.1:n.439+4959T>G
ENST00000641434.1:c.744T>G	ENSP00000493279.1:p.Asn248Lys
ENST00000641464.1:c.449+1060T>G	ENSP00000493438.1:n.449+1060T>G
ENST00000641482.1:c.744T>G	ENSP00000493277.1:p.Asn248Lys
ENST00000641503.1:c.630T>G	ENSP00000493304.1:p.Asn210Lys
ENST00000641508.1:c.698+1060T>G	ENSP00000493209.1:n.698+1060T>G
ENST00000641509.1:c.439+4959T>G	ENSP00000493459.1:n.439+4959T>G
ENST00000641538.1:c.590T>G
ENST00000641590.1:c.630T>G	ENSP00000493132.1:p.Asn210Lys
ENST00000641658.1:c.464T>G	ENSP00000492987.1:p.Ile155Ser
ENST00000641686.2:c.744T>G MANE Select	ENSP00000493218.2:p.Asn248Lys
ENST00000641690.1:c.553+3252T>G	ENSP00000492966.1:n.553+3252T>G
ENST00000641695.1:c.*28T>G	ENSP00000493134.1:n.*28T>G
ENST00000641742.1:c.599T>G	ENSP00000493315.1:p.Ile200Ser
ENST00000641743.1:c.744T>G	ENSP00000493130.1:p.Asn248Lys
ENST00000641748.1:c.744T>G	ENSP00000493330.1:p.Asn248Lys
ENST00000641753.1:c.571T>G
ENST00000641774.1:c.584+1060T>G	ENSP00000492960.1:n.584+1060T>G
ENST00000641776.1:c.*296T>G	ENSP00000493261.1:n.*296T>G
ENST00000641830.1:c.80T>G
ENST00000641843.1:c.350T>G	ENSP00000493174.1:p.Ile117Ser
ENST00000641869.1:c.49T>G
ENST00000641870.1:c.599T>G	ENSP00000493044.1:p.Ile200Ser
ENST00000641882.1:c.485T>G	ENSP00000493301.1:p.Ile162Ser
ENST00000641928.1:c.449+1060T>G	ENSP00000493418.1:n.449+1060T>G
ENST00000641949.1:c.553+3252T>G	ENSP00000492891.1:n.553+3252T>G
ENST00000642012.1:n.608T>G
ENST00000642034.1:c.630T>G	ENSP00000493285.1:p.Asn210Lys
ENST00000642042.1:c.744T>G	ENSP00000493260.1:p.Asn248Lys
ENST00000642078.1:c.464T>G	ENSP00000492885.1:p.Ile155Ser
ENST00000642121.1:n.91-7976T>G
ENST00000296468.7:c.744T>G	ENSP00000296468.3:p.Asn248Lys
ENST00000505284.5:n.639T>G
ENST00000508441.1:n.611T>G
ENST00000509826.1:c.449+1060T>G	ENSP00000421176.1:n.449+1060T>G
ENST00000513559.5:c.609T>G	ENSP00000425000.1:p.Asn203Lys
ENST00000515130.5:n.1190T>G
NM_152778.2:c.744T>G	NP_689991.1:p.Asn248Lys
XM_005262893.1:c.744T>G	XP_005262950.1:p.Asn248Lys
XM_005262896.1:c.597T>G	XP_005262953.1:p.Asn199Lys
XM_005262897.1:c.553+3252T>G	XP_005262954.1:n.553+3252T>G
XM_005262898.2:c.744T>G	XP_005262955.1:p.Asn248Lys
XM_005262900.2:c.599T>G	XP_005262957.1:p.Ile200Ser
XM_011531830.1:c.630T>G	XP_011530132.1:p.Asn210Lys
XM_011531831.1:c.439+4959T>G	XP_011530133.1:n.439+4959T>G
XM_011531832.1:c.630T>G	XP_011530134.1:p.Asn210Lys
XR_938717.1:n.821T>G
NM_001363520.1:c.553+3252T>G	NP_001350449.1:n.553+3252T>G
NM_001363521.1:c.439+4959T>G	NP_001350450.1:n.439+4959T>G
XM_005262898.3:c.744T>G	XP_005262955.1:p.Asn248Lys
XM_017007989.1:c.553+3252T>G	XP_016863478.1:n.553+3252T>G
XM_024453981.1:c.609T>G	XP_024309749.1:p.Asn203Lys
XM_024453982.1:c.495T>G	XP_024309750.1:p.Asn165Lys
XM_024453983.1:c.304+4959T>G	XP_024309751.1:n.304+4959T>G
XR_001741194.1:n.821T>G
XR_001741195.1:n.707T>G
XR_001741196.1:n.630+3252T>G
XR_001741197.1:n.676T>G
XR_001741198.2:n.676T>G
XR_001741199.1:n.676T>G
XR_938717.2:n.821T>G
NM_001363520.2:c.553+3252T>G	NP_001350449.1:n.553+3252T>G
NM_001363521.2:c.439+4959T>G	NP_001350450.1:n.439+4959T>G
NM_001371590.1:c.609T>G	NP_001358519.1:p.Asn203Lys
NM_001371591.1:c.744T>G	NP_001358520.1:p.Asn248Lys
NM_001371592.1:c.750T>G	NP_001358521.1:p.Asn250Lys
NM_001371593.1:c.630T>G	NP_001358522.1:p.Asn210Lys
NM_001371594.1:c.597T>G	NP_001358523.1:p.Asn199Lys
NM_001371595.1:c.462T>G	NP_001358524.1:p.Asn154Lys
NM_001371596.2:c.744T>G MANE Select	NP_001358525.1:p.Asn248Lys
NM_152778.3:c.744T>G	NP_689991.1:p.Asn248Lys
NM_152778.4:c.744T>G	NP_689991.1:p.Asn248Lys