Canonical Allele Identifier: CA1492804112
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921606G= , CM000666.2:g.127921606G= GRCh38
NC_000004.11:g.128842761G= , CM000666.1:g.128842761G= GRCh37
NC_000004.10:g.129062211G= NCBI36
NG_008657.1:g.49379C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1268C= ENSP00000296468.3:p.Ala423=
ENST00000509826.2:c.*589C= ENSP00000421176.2:n.*589C=
ENST00000513559.6:c.986C= ENSP00000425000.2:p.Ala329=
ENST00000515130.6:c.*153C= ENSP00000493056.1:n.*153C=
ENST00000641025.1:c.*153C= ENSP00000493346.1:n.*153C=
ENST00000641092.1:c.*153C= ENSP00000493392.1:n.*153C=
ENST00000641133.1:c.*582C= ENSP00000493192.1:n.*582C=
ENST00000641146.1:n.1134C=
ENST00000641147.1:c.818C= ENSP00000493133.1:p.Ala273=
ENST00000641178.1:c.1133C= ENSP00000492989.1:p.Ala378=
ENST00000641186.1:c.1154C= ENSP00000493347.1:p.Ala385=
ENST00000641228.1:c.*153C= ENSP00000493194.1:n.*153C=
ENST00000641332.1:c.*329C= ENSP00000493397.1:n.*329C=
ENST00000641340.1:c.*397C= ENSP00000493191.1:n.*397C=
ENST00000641388.1:n.515C=
ENST00000641393.1:c.818C= ENSP00000493197.1:p.Ala273=
ENST00000641397.1:c.*153C= ENSP00000493406.1:n.*153C=
ENST00000641413.1:c.193C=
ENST00000641434.1:c.1268C= ENSP00000493279.1:p.Ala423=
ENST00000641464.1:c.*501C= ENSP00000493438.1:n.*501C=
ENST00000641482.1:c.*153C= ENSP00000493277.1:n.*153C=
ENST00000641508.1:c.*501C= ENSP00000493209.1:n.*501C=
ENST00000641509.1:c.953C= ENSP00000493459.1:p.Ala318=
ENST00000641590.1:c.*153C= ENSP00000493132.1:n.*153C=
ENST00000641658.1:c.*433C= ENSP00000492987.1:n.*433C=
ENST00000641686.2:c.1268C= MANE Select ENSP00000493218.2:p.Ala423=
ENST00000641690.1:c.1067C= ENSP00000492966.1:p.Ala356=
ENST00000641742.1:c.*433C= ENSP00000493315.1:n.*433C=
ENST00000641748.1:c.1268C= ENSP00000493330.1:p.Ala423=
ENST00000641753.1:c.1095C=
ENST00000641774.1:c.*520C= ENSP00000492960.1:n.*520C=
ENST00000641830.1:c.500C=
ENST00000641843.1:c.*329C= ENSP00000493174.1:n.*329C=
ENST00000641869.1:c.469C=
ENST00000641870.1:c.*329C= ENSP00000493044.1:n.*329C=
ENST00000641882.1:c.*433C= ENSP00000493301.1:n.*433C=
ENST00000641928.1:c.*397C= ENSP00000493418.1:n.*397C=
ENST00000641949.1:c.554-770C= ENSP00000492891.1:n.554-770C=
ENST00000642012.1:n.1132C=
ENST00000642034.1:c.*153C= ENSP00000493285.1:n.*153C=
ENST00000642042.1:c.1268C= ENSP00000493260.1:p.Ala423=
ENST00000642078.1:c.*329C= ENSP00000492885.1:n.*329C=
ENST00000296468.7:c.1268C= ENSP00000296468.3:p.Ala423=
ENST00000504126.1:n.296C=
ENST00000513559.5:c.1133C= ENSP00000425000.1:p.Ala378=
ENST00000515130.5:n.1610C=
NM_152778.2:c.1268C= NP_689991.1:p.Ala423=
XM_005262893.1:c.1268C= XP_005262950.1:p.Ala423=
XM_005262896.1:c.1121C= XP_005262953.1:p.Ala374=
XM_005262897.1:c.1067C= XP_005262954.1:p.Ala356=
XM_005262898.2:c.*153C= XP_005262955.1:n.*153C=
XM_011531830.1:c.1154C= XP_011530132.1:p.Ala385=
XM_011531831.1:c.953C= XP_011530133.1:p.Ala318=
XM_011531832.1:c.*153C= XP_011530134.1:n.*153C=
XR_938717.1:n.1345C=
NM_001363520.1:c.1067C= NP_001350449.1:p.Ala356=
NM_001363521.1:c.953C= NP_001350450.1:p.Ala318=
XM_005262898.3:c.*153C= XP_005262955.1:n.*153C=
XM_017007989.1:c.*153C= XP_016863478.1:n.*153C=
XM_024453981.1:c.1133C= XP_024309749.1:p.Ala378=
XM_024453982.1:c.1019C= XP_024309750.1:p.Ala340=
XM_024453983.1:c.818C= XP_024309751.1:p.Ala273=
XR_001741194.1:n.1241C=
XR_001741195.1:n.1127C=
XR_001741196.1:n.1040C=
XR_001741197.1:n.1200C=
XR_001741198.2:n.1096C=
XR_001741199.1:n.1096C=
XR_938717.2:n.1345C=
NM_001363520.2:c.1067C= NP_001350449.1:p.Ala356=
NM_001363521.2:c.953C= NP_001350450.1:p.Ala318=
NM_001371590.1:c.1133C= NP_001358519.1:p.Ala378=
NM_001371591.1:c.1268C= NP_001358520.1:p.Ala423=
NM_001371592.1:c.1274C= NP_001358521.1:p.Ala425=
NM_001371593.1:c.1154C= NP_001358522.1:p.Ala385=
NM_001371594.1:c.1121C= NP_001358523.1:p.Ala374=
NM_001371595.1:c.986C= NP_001358524.1:p.Ala329=
NM_001371596.2:c.1268C= MANE Select NP_001358525.1:p.Ala423=
NM_152778.3:c.1268C= NP_689991.1:p.Ala423=
NM_152778.4:c.1268C= NP_689991.1:p.Ala423=