Canonical Allele Identifier: CA358171082

Gene: MFSD8

Linked Data

• MyVariant Identifiers: chr4:g.128842738G>A (hg19) ; chr4:g.127921583G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921583G>A , CM000666.2:g.127921583G>A	GRCh38
NC_000004.11:g.128842738G>A , CM000666.1:g.128842738G>A	GRCh37
NC_000004.10:g.129062188G>A	NCBI36
NG_008657.1:g.49402C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1291C>T	ENSP00000296468.3:p.Pro431Ser
ENST00000509826.2:c.*612C>T	ENSP00000421176.2:n.*612C>T
ENST00000513559.6:c.1009C>T	ENSP00000425000.2:p.Pro337Ser
ENST00000515130.6:c.*176C>T	ENSP00000493056.1:n.*176C>T
ENST00000641025.1:c.*176C>T	ENSP00000493346.1:n.*176C>T
ENST00000641092.1:c.*176C>T	ENSP00000493392.1:n.*176C>T
ENST00000641133.1:c.*605C>T	ENSP00000493192.1:n.*605C>T
ENST00000641146.1:n.1157C>T
ENST00000641147.1:c.841C>T	ENSP00000493133.1:p.Pro281Ser
ENST00000641178.1:c.1156C>T	ENSP00000492989.1:p.Pro386Ser
ENST00000641186.1:c.1177C>T	ENSP00000493347.1:p.Pro393Ser
ENST00000641228.1:c.*176C>T	ENSP00000493194.1:n.*176C>T
ENST00000641332.1:c.*352C>T	ENSP00000493397.1:n.*352C>T
ENST00000641340.1:c.*420C>T	ENSP00000493191.1:n.*420C>T
ENST00000641388.1:n.538C>T
ENST00000641393.1:c.841C>T	ENSP00000493197.1:p.Pro281Ser
ENST00000641397.1:c.*176C>T	ENSP00000493406.1:n.*176C>T
ENST00000641413.1:c.216C>T
ENST00000641434.1:c.1291C>T	ENSP00000493279.1:p.Pro431Ser
ENST00000641464.1:c.*524C>T	ENSP00000493438.1:n.*524C>T
ENST00000641482.1:c.*176C>T	ENSP00000493277.1:n.*176C>T
ENST00000641508.1:c.*524C>T	ENSP00000493209.1:n.*524C>T
ENST00000641509.1:c.976C>T	ENSP00000493459.1:p.Pro326Ser
ENST00000641590.1:c.*176C>T	ENSP00000493132.1:n.*176C>T
ENST00000641658.1:c.*456C>T	ENSP00000492987.1:n.*456C>T
ENST00000641686.2:c.1291C>T MANE Select	ENSP00000493218.2:p.Pro431Ser
ENST00000641690.1:c.1090C>T	ENSP00000492966.1:p.Pro364Ser
ENST00000641742.1:c.*456C>T	ENSP00000493315.1:n.*456C>T
ENST00000641748.1:c.1291C>T	ENSP00000493330.1:p.Pro431Ser
ENST00000641753.1:c.1118C>T
ENST00000641774.1:c.*543C>T	ENSP00000492960.1:n.*543C>T
ENST00000641830.1:c.523C>T
ENST00000641843.1:c.*352C>T	ENSP00000493174.1:n.*352C>T
ENST00000641869.1:c.492C>T
ENST00000641870.1:c.*352C>T	ENSP00000493044.1:n.*352C>T
ENST00000641882.1:c.*456C>T	ENSP00000493301.1:n.*456C>T
ENST00000641928.1:c.*420C>T	ENSP00000493418.1:n.*420C>T
ENST00000641949.1:c.554-747C>T	ENSP00000492891.1:n.554-747C>T
ENST00000642012.1:n.1155C>T
ENST00000642034.1:c.*176C>T	ENSP00000493285.1:n.*176C>T
ENST00000642042.1:c.1291C>T	ENSP00000493260.1:p.Pro431Ser
ENST00000642078.1:c.*352C>T	ENSP00000492885.1:n.*352C>T
ENST00000296468.7:c.1291C>T	ENSP00000296468.3:p.Pro431Ser
ENST00000504126.1:n.319C>T
ENST00000513559.5:c.1156C>T	ENSP00000425000.1:p.Pro386Ser
ENST00000515130.5:n.1633C>T
NM_152778.2:c.1291C>T	NP_689991.1:p.Pro431Ser
XM_005262893.1:c.1291C>T	XP_005262950.1:p.Pro431Ser
XM_005262896.1:c.1144C>T	XP_005262953.1:p.Pro382Ser
XM_005262897.1:c.1090C>T	XP_005262954.1:p.Pro364Ser
XM_005262898.2:c.*176C>T	XP_005262955.1:n.*176C>T
XM_011531830.1:c.1177C>T	XP_011530132.1:p.Pro393Ser
XM_011531831.1:c.976C>T	XP_011530133.1:p.Pro326Ser
XM_011531832.1:c.*176C>T	XP_011530134.1:n.*176C>T
XR_938717.1:n.1368C>T
NM_001363520.1:c.1090C>T	NP_001350449.1:p.Pro364Ser
NM_001363521.1:c.976C>T	NP_001350450.1:p.Pro326Ser
XM_005262898.3:c.*176C>T	XP_005262955.1:n.*176C>T
XM_017007989.1:c.*176C>T	XP_016863478.1:n.*176C>T
XM_024453981.1:c.1156C>T	XP_024309749.1:p.Pro386Ser
XM_024453982.1:c.1042C>T	XP_024309750.1:p.Pro348Ser
XM_024453983.1:c.841C>T	XP_024309751.1:p.Pro281Ser
XR_001741194.1:n.1264C>T
XR_001741195.1:n.1150C>T
XR_001741196.1:n.1063C>T
XR_001741197.1:n.1223C>T
XR_001741198.2:n.1119C>T
XR_001741199.1:n.1119C>T
XR_938717.2:n.1368C>T
NM_001363520.2:c.1090C>T	NP_001350449.1:p.Pro364Ser
NM_001363521.2:c.976C>T	NP_001350450.1:p.Pro326Ser
NM_001371590.1:c.1156C>T	NP_001358519.1:p.Pro386Ser
NM_001371591.1:c.1291C>T	NP_001358520.1:p.Pro431Ser
NM_001371592.1:c.1297C>T	NP_001358521.1:p.Pro433Ser
NM_001371593.1:c.1177C>T	NP_001358522.1:p.Pro393Ser
NM_001371594.1:c.1144C>T	NP_001358523.1:p.Pro382Ser
NM_001371595.1:c.1009C>T	NP_001358524.1:p.Pro337Ser
NM_001371596.2:c.1291C>T MANE Select	NP_001358525.1:p.Pro431Ser
NM_152778.3:c.1291C>T	NP_689991.1:p.Pro431Ser
NM_152778.4:c.1291C>T	NP_689991.1:p.Pro431Ser