Canonical Allele Identifier: CA358176373

Gene: MFSD8

Linked Data

• COSMIC: COSM71631
• MyVariant Identifiers: chr4:g.128863278C>T (hg19) ; chr4:g.127942123C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127942123C>T , CM000666.2:g.127942123C>T	GRCh38
NC_000004.11:g.128863278C>T , CM000666.1:g.128863278C>T	GRCh37
NC_000004.10:g.129082728C>T	NCBI36
NG_008657.1:g.28862G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.475G>A	ENSP00000296468.3:p.Ala159Thr
ENST00000505284.6:n.691G>A
ENST00000508441.2:n.490G>A
ENST00000509826.2:c.475G>A	ENSP00000421176.2:p.Ala159Thr
ENST00000513559.6:c.340G>A	ENSP00000425000.2:p.Ala114Thr
ENST00000515130.6:c.340G>A	ENSP00000493056.1:p.Ala114Thr
ENST00000641025.1:c.475G>A	ENSP00000493346.1:p.Ala159Thr
ENST00000641092.1:c.475G>A	ENSP00000493392.1:p.Ala159Thr
ENST00000641133.1:c.475G>A	ENSP00000493192.1:p.Ala159Thr
ENST00000641134.1:c.340G>A	ENSP00000492925.1:p.Ala114Thr
ENST00000641147.1:c.304+1629G>A	ENSP00000493133.1:n.304+1629G>A
ENST00000641178.1:c.340G>A	ENSP00000492989.1:p.Ala114Thr
ENST00000641186.1:c.439+1629G>A	ENSP00000493347.1:n.439+1629G>A
ENST00000641228.1:c.475G>A	ENSP00000493194.1:p.Ala159Thr
ENST00000641243.1:c.475G>A	ENSP00000493083.1:p.Ala159Thr
ENST00000641264.1:c.*272G>A	ENSP00000492908.1:n.*272G>A
ENST00000641332.1:c.475G>A	ENSP00000493397.1:p.Ala159Thr
ENST00000641340.1:c.475G>A	ENSP00000493191.1:p.Ala159Thr
ENST00000641369.1:c.-30G>A	ENSP00000493037.1:n.-30G>A
ENST00000641393.1:c.304+1629G>A	ENSP00000493197.1:n.304+1629G>A
ENST00000641397.1:c.439+1629G>A	ENSP00000493406.1:n.439+1629G>A
ENST00000641434.1:c.475G>A	ENSP00000493279.1:p.Ala159Thr
ENST00000641464.1:c.304+1629G>A	ENSP00000493438.1:n.304+1629G>A
ENST00000641482.1:c.475G>A	ENSP00000493277.1:p.Ala159Thr
ENST00000641503.1:c.439+1629G>A	ENSP00000493304.1:n.439+1629G>A
ENST00000641508.1:c.475G>A	ENSP00000493209.1:p.Ala159Thr
ENST00000641509.1:c.439+1629G>A	ENSP00000493459.1:n.439+1629G>A
ENST00000641538.1:c.321G>A
ENST00000641558.1:c.331G>A	ENSP00000493335.1:p.Ala111Thr
ENST00000641590.1:c.439+1629G>A	ENSP00000493132.1:n.439+1629G>A
ENST00000641658.1:c.340G>A	ENSP00000492987.1:p.Ala114Thr
ENST00000641686.2:c.475G>A MANE Select	ENSP00000493218.2:p.Ala159Thr
ENST00000641690.1:c.475G>A	ENSP00000492966.1:p.Ala159Thr
ENST00000641695.1:c.475G>A	ENSP00000493134.1:p.Ala159Thr
ENST00000641742.1:c.475G>A	ENSP00000493315.1:p.Ala159Thr
ENST00000641743.1:c.475G>A	ENSP00000493130.1:p.Ala159Thr
ENST00000641748.1:c.475G>A	ENSP00000493330.1:p.Ala159Thr
ENST00000641753.1:c.380+1629G>A
ENST00000641774.1:c.439+1629G>A	ENSP00000492960.1:n.439+1629G>A
ENST00000641776.1:c.*27G>A	ENSP00000493261.1:n.*27G>A
ENST00000641843.1:c.304+1629G>A	ENSP00000493174.1:n.304+1629G>A
ENST00000641870.1:c.475G>A	ENSP00000493044.1:p.Ala159Thr
ENST00000641882.1:c.439+1629G>A	ENSP00000493301.1:n.439+1629G>A
ENST00000641928.1:c.304+1629G>A	ENSP00000493418.1:n.304+1629G>A
ENST00000641949.1:c.475G>A	ENSP00000492891.1:p.Ala159Thr
ENST00000642034.1:c.439+1629G>A	ENSP00000493285.1:n.439+1629G>A
ENST00000642042.1:c.475G>A	ENSP00000493260.1:p.Ala159Thr
ENST00000642078.1:c.340G>A	ENSP00000492885.1:p.Ala114Thr
ENST00000642121.1:n.91-11306G>A
ENST00000642143.1:n.320G>A
ENST00000296468.7:c.475G>A	ENSP00000296468.3:p.Ala159Thr
ENST00000505284.5:n.448+1629G>A
ENST00000508441.1:n.487G>A
ENST00000509826.1:c.304+1629G>A	ENSP00000421176.1:n.304+1629G>A
ENST00000513559.5:c.340G>A	ENSP00000425000.1:p.Ala114Thr
ENST00000515130.5:n.921G>A
NM_152778.2:c.475G>A	NP_689991.1:p.Ala159Thr
XM_005262893.1:c.475G>A	XP_005262950.1:p.Ala159Thr
XM_005262896.1:c.475G>A	XP_005262953.1:p.Ala159Thr
XM_005262897.1:c.475G>A	XP_005262954.1:p.Ala159Thr
XM_005262898.2:c.475G>A	XP_005262955.1:p.Ala159Thr
XM_005262900.2:c.475G>A	XP_005262957.1:p.Ala159Thr
XM_011531830.1:c.439+1629G>A	XP_011530132.1:n.439+1629G>A
XM_011531831.1:c.439+1629G>A	XP_011530133.1:n.439+1629G>A
XM_011531832.1:c.439+1629G>A	XP_011530134.1:n.439+1629G>A
XR_938717.1:n.552G>A
NM_001363520.1:c.475G>A	NP_001350449.1:p.Ala159Thr
NM_001363521.1:c.439+1629G>A	NP_001350450.1:n.439+1629G>A
XM_005262898.3:c.475G>A	XP_005262955.1:p.Ala159Thr
XM_017007989.1:c.475G>A	XP_016863478.1:p.Ala159Thr
XM_024453981.1:c.340G>A	XP_024309749.1:p.Ala114Thr
XM_024453982.1:c.304+1629G>A	XP_024309750.1:n.304+1629G>A
XM_024453983.1:c.304+1629G>A	XP_024309751.1:n.304+1629G>A
XR_001741194.1:n.552G>A
XR_001741195.1:n.516+1629G>A
XR_001741196.1:n.552G>A
XR_001741197.1:n.552G>A
XR_001741198.2:n.552G>A
XR_001741199.1:n.552G>A
XR_938717.2:n.552G>A
NM_001363520.2:c.475G>A	NP_001350449.1:p.Ala159Thr
NM_001363521.2:c.439+1629G>A	NP_001350450.1:n.439+1629G>A
NM_001371590.1:c.340G>A	NP_001358519.1:p.Ala114Thr
NM_001371591.1:c.475G>A	NP_001358520.1:p.Ala159Thr
NM_001371592.1:c.475G>A	NP_001358521.1:p.Ala159Thr
NM_001371593.1:c.439+1629G>A	NP_001358522.1:n.439+1629G>A
NM_001371594.1:c.475G>A	NP_001358523.1:p.Ala159Thr
NM_001371595.1:c.340G>A	NP_001358524.1:p.Ala114Thr
NM_001371596.2:c.475G>A MANE Select	NP_001358525.1:p.Ala159Thr
NM_152778.3:c.475G>A	NP_689991.1:p.Ala159Thr
NM_152778.4:c.475G>A	NP_689991.1:p.Ala159Thr