Canonical Allele Identifier: CA1492804135
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921617G= , CM000666.2:g.127921617G= GRCh38
NC_000004.11:g.128842772G= , CM000666.1:g.128842772G= GRCh37
NC_000004.10:g.129062222G= NCBI36
NG_008657.1:g.49368C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1257C= ENSP00000296468.3:p.Phe419=
ENST00000509826.2:c.*578C= ENSP00000421176.2:n.*578C=
ENST00000513559.6:c.975C= ENSP00000425000.2:p.Phe325=
ENST00000515130.6:c.*142C= ENSP00000493056.1:n.*142C=
ENST00000641025.1:c.*142C= ENSP00000493346.1:n.*142C=
ENST00000641092.1:c.*142C= ENSP00000493392.1:n.*142C=
ENST00000641133.1:c.*571C= ENSP00000493192.1:n.*571C=
ENST00000641146.1:n.1123C=
ENST00000641147.1:c.807C= ENSP00000493133.1:p.Phe269=
ENST00000641178.1:c.1122C= ENSP00000492989.1:p.Phe374=
ENST00000641186.1:c.1143C= ENSP00000493347.1:p.Phe381=
ENST00000641228.1:c.*142C= ENSP00000493194.1:n.*142C=
ENST00000641332.1:c.*318C= ENSP00000493397.1:n.*318C=
ENST00000641340.1:c.*386C= ENSP00000493191.1:n.*386C=
ENST00000641388.1:n.504C=
ENST00000641393.1:c.807C= ENSP00000493197.1:p.Phe269=
ENST00000641397.1:c.*142C= ENSP00000493406.1:n.*142C=
ENST00000641413.1:c.182C=
ENST00000641434.1:c.1257C= ENSP00000493279.1:p.Phe419=
ENST00000641464.1:c.*490C= ENSP00000493438.1:n.*490C=
ENST00000641482.1:c.*142C= ENSP00000493277.1:n.*142C=
ENST00000641508.1:c.*490C= ENSP00000493209.1:n.*490C=
ENST00000641509.1:c.942C= ENSP00000493459.1:p.Phe314=
ENST00000641590.1:c.*142C= ENSP00000493132.1:n.*142C=
ENST00000641658.1:c.*422C= ENSP00000492987.1:n.*422C=
ENST00000641686.2:c.1257C= MANE Select ENSP00000493218.2:p.Phe419=
ENST00000641690.1:c.1056C= ENSP00000492966.1:p.Phe352=
ENST00000641742.1:c.*422C= ENSP00000493315.1:n.*422C=
ENST00000641748.1:c.1257C= ENSP00000493330.1:p.Phe419=
ENST00000641753.1:c.1084C=
ENST00000641774.1:c.*509C= ENSP00000492960.1:n.*509C=
ENST00000641830.1:c.489C=
ENST00000641843.1:c.*318C= ENSP00000493174.1:n.*318C=
ENST00000641869.1:c.458C=
ENST00000641870.1:c.*318C= ENSP00000493044.1:n.*318C=
ENST00000641882.1:c.*422C= ENSP00000493301.1:n.*422C=
ENST00000641928.1:c.*386C= ENSP00000493418.1:n.*386C=
ENST00000641949.1:c.554-781C= ENSP00000492891.1:n.554-781C=
ENST00000642012.1:n.1121C=
ENST00000642034.1:c.*142C= ENSP00000493285.1:n.*142C=
ENST00000642042.1:c.1257C= ENSP00000493260.1:p.Phe419=
ENST00000642078.1:c.*318C= ENSP00000492885.1:n.*318C=
ENST00000296468.7:c.1257C= ENSP00000296468.3:p.Phe419=
ENST00000504126.1:n.285C=
ENST00000513559.5:c.1122C= ENSP00000425000.1:p.Phe374=
ENST00000515130.5:n.1599C=
NM_152778.2:c.1257C= NP_689991.1:p.Phe419=
XM_005262893.1:c.1257C= XP_005262950.1:p.Phe419=
XM_005262896.1:c.1110C= XP_005262953.1:p.Phe370=
XM_005262897.1:c.1056C= XP_005262954.1:p.Phe352=
XM_005262898.2:c.*142C= XP_005262955.1:n.*142C=
XM_011531830.1:c.1143C= XP_011530132.1:p.Phe381=
XM_011531831.1:c.942C= XP_011530133.1:p.Phe314=
XM_011531832.1:c.*142C= XP_011530134.1:n.*142C=
XR_938717.1:n.1334C=
NM_001363520.1:c.1056C= NP_001350449.1:p.Phe352=
NM_001363521.1:c.942C= NP_001350450.1:p.Phe314=
XM_005262898.3:c.*142C= XP_005262955.1:n.*142C=
XM_017007989.1:c.*142C= XP_016863478.1:n.*142C=
XM_024453981.1:c.1122C= XP_024309749.1:p.Phe374=
XM_024453982.1:c.1008C= XP_024309750.1:p.Phe336=
XM_024453983.1:c.807C= XP_024309751.1:p.Phe269=
XR_001741194.1:n.1230C=
XR_001741195.1:n.1116C=
XR_001741196.1:n.1029C=
XR_001741197.1:n.1189C=
XR_001741198.2:n.1085C=
XR_001741199.1:n.1085C=
XR_938717.2:n.1334C=
NM_001363520.2:c.1056C= NP_001350449.1:p.Phe352=
NM_001363521.2:c.942C= NP_001350450.1:p.Phe314=
NM_001371590.1:c.1122C= NP_001358519.1:p.Phe374=
NM_001371591.1:c.1257C= NP_001358520.1:p.Phe419=
NM_001371592.1:c.1263C= NP_001358521.1:p.Phe421=
NM_001371593.1:c.1143C= NP_001358522.1:p.Phe381=
NM_001371594.1:c.1110C= NP_001358523.1:p.Phe370=
NM_001371595.1:c.975C= NP_001358524.1:p.Phe325=
NM_001371596.2:c.1257C= MANE Select NP_001358525.1:p.Phe419=
NM_152778.3:c.1257C= NP_689991.1:p.Phe419=
NM_152778.4:c.1257C= NP_689991.1:p.Phe419=