Canonical Allele Identifier: CA1492804048
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921564G= , CM000666.2:g.127921564G= GRCh38
NC_000004.11:g.128842719G= , CM000666.1:g.128842719G= GRCh37
NC_000004.10:g.129062169G= NCBI36
NG_008657.1:g.49421C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1310C= ENSP00000296468.3:p.Ser437=
ENST00000509826.2:c.*631C= ENSP00000421176.2:n.*631C=
ENST00000513559.6:c.1028C= ENSP00000425000.2:p.Ser343=
ENST00000515130.6:c.*195C= ENSP00000493056.1:n.*195C=
ENST00000641025.1:c.*195C= ENSP00000493346.1:n.*195C=
ENST00000641092.1:c.*195C= ENSP00000493392.1:n.*195C=
ENST00000641133.1:c.*624C= ENSP00000493192.1:n.*624C=
ENST00000641146.1:n.1176C=
ENST00000641147.1:c.860C= ENSP00000493133.1:p.Ser287=
ENST00000641178.1:c.1175C= ENSP00000492989.1:p.Ser392=
ENST00000641186.1:c.1196C= ENSP00000493347.1:p.Ser399=
ENST00000641228.1:c.*195C= ENSP00000493194.1:n.*195C=
ENST00000641332.1:c.*371C= ENSP00000493397.1:n.*371C=
ENST00000641340.1:c.*439C= ENSP00000493191.1:n.*439C=
ENST00000641388.1:n.557C=
ENST00000641393.1:c.860C= ENSP00000493197.1:p.Ser287=
ENST00000641397.1:c.*195C= ENSP00000493406.1:n.*195C=
ENST00000641413.1:c.235C=
ENST00000641434.1:c.1310C= ENSP00000493279.1:p.Ser437=
ENST00000641464.1:c.*543C= ENSP00000493438.1:n.*543C=
ENST00000641482.1:c.*195C= ENSP00000493277.1:n.*195C=
ENST00000641508.1:c.*543C= ENSP00000493209.1:n.*543C=
ENST00000641509.1:c.995C= ENSP00000493459.1:p.Ser332=
ENST00000641590.1:c.*195C= ENSP00000493132.1:n.*195C=
ENST00000641658.1:c.*475C= ENSP00000492987.1:n.*475C=
ENST00000641686.2:c.1310C= MANE Select ENSP00000493218.2:p.Ser437=
ENST00000641690.1:c.1109C= ENSP00000492966.1:p.Ser370=
ENST00000641742.1:c.*475C= ENSP00000493315.1:n.*475C=
ENST00000641748.1:c.1310C= ENSP00000493330.1:p.Ser437=
ENST00000641753.1:c.1137C=
ENST00000641774.1:c.*562C= ENSP00000492960.1:n.*562C=
ENST00000641830.1:c.542C=
ENST00000641843.1:c.*371C= ENSP00000493174.1:n.*371C=
ENST00000641869.1:c.511C=
ENST00000641870.1:c.*371C= ENSP00000493044.1:n.*371C=
ENST00000641882.1:c.*475C= ENSP00000493301.1:n.*475C=
ENST00000641928.1:c.*439C= ENSP00000493418.1:n.*439C=
ENST00000641949.1:c.554-728C= ENSP00000492891.1:n.554-728C=
ENST00000642012.1:n.1174C=
ENST00000642034.1:c.*195C= ENSP00000493285.1:n.*195C=
ENST00000642042.1:c.1310C= ENSP00000493260.1:p.Ser437=
ENST00000642078.1:c.*371C= ENSP00000492885.1:n.*371C=
ENST00000296468.7:c.1310C= ENSP00000296468.3:p.Ser437=
ENST00000504126.1:n.338C=
ENST00000513559.5:c.1175C= ENSP00000425000.1:p.Ser392=
ENST00000515130.5:n.1652C=
NM_152778.2:c.1310C= NP_689991.1:p.Ser437=
XM_005262893.1:c.1310C= XP_005262950.1:p.Ser437=
XM_005262896.1:c.1163C= XP_005262953.1:p.Ser388=
XM_005262897.1:c.1109C= XP_005262954.1:p.Ser370=
XM_005262898.2:c.*195C= XP_005262955.1:n.*195C=
XM_011531830.1:c.1196C= XP_011530132.1:p.Ser399=
XM_011531831.1:c.995C= XP_011530133.1:p.Ser332=
XM_011531832.1:c.*195C= XP_011530134.1:n.*195C=
XR_938717.1:n.1387C=
NM_001363520.1:c.1109C= NP_001350449.1:p.Ser370=
NM_001363521.1:c.995C= NP_001350450.1:p.Ser332=
XM_005262898.3:c.*195C= XP_005262955.1:n.*195C=
XM_017007989.1:c.*195C= XP_016863478.1:n.*195C=
XM_024453981.1:c.1175C= XP_024309749.1:p.Ser392=
XM_024453982.1:c.1061C= XP_024309750.1:p.Ser354=
XM_024453983.1:c.860C= XP_024309751.1:p.Ser287=
XR_001741194.1:n.1283C=
XR_001741195.1:n.1169C=
XR_001741196.1:n.1082C=
XR_001741197.1:n.1242C=
XR_001741198.2:n.1138C=
XR_001741199.1:n.1138C=
XR_938717.2:n.1387C=
NM_001363520.2:c.1109C= NP_001350449.1:p.Ser370=
NM_001363521.2:c.995C= NP_001350450.1:p.Ser332=
NM_001371590.1:c.1175C= NP_001358519.1:p.Ser392=
NM_001371591.1:c.1310C= NP_001358520.1:p.Ser437=
NM_001371592.1:c.1316C= NP_001358521.1:p.Ser439=
NM_001371593.1:c.1196C= NP_001358522.1:p.Ser399=
NM_001371594.1:c.1163C= NP_001358523.1:p.Ser388=
NM_001371595.1:c.1028C= NP_001358524.1:p.Ser343=
NM_001371596.2:c.1310C= MANE Select NP_001358525.1:p.Ser437=
NM_152778.3:c.1310C= NP_689991.1:p.Ser437=
NM_152778.4:c.1310C= NP_689991.1:p.Ser437=