Canonical Allele Identifier: CA1492817159
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921494A= , CM000666.2:g.127921494A= GRCh38
NC_000004.11:g.128842649A= , CM000666.1:g.128842649A= GRCh37
NC_000004.10:g.129062099A= NCBI36
NG_008657.1:g.49491T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1350+30T= ENSP00000296468.3:n.1350+30T=
ENST00000509826.2:c.*671+30T= ENSP00000421176.2:n.*671+30T=
ENST00000513559.6:c.1068+30T= ENSP00000425000.2:n.1068+30T=
ENST00000515130.6:c.*235+30T= ENSP00000493056.1:n.*235+30T=
ENST00000641025.1:c.*235+30T= ENSP00000493346.1:n.*235+30T=
ENST00000641092.1:c.*235+30T= ENSP00000493392.1:n.*235+30T=
ENST00000641133.1:c.*694T= ENSP00000493192.1:n.*694T=
ENST00000641146.1:n.1246T=
ENST00000641147.1:c.900+30T= ENSP00000493133.1:n.900+30T=
ENST00000641178.1:c.1215+30T= ENSP00000492989.1:n.1215+30T=
ENST00000641186.1:c.1236+30T= ENSP00000493347.1:n.1236+30T=
ENST00000641228.1:c.*265T= ENSP00000493194.1:n.*265T=
ENST00000641332.1:c.*411+30T= ENSP00000493397.1:n.*411+30T=
ENST00000641340.1:c.*509T= ENSP00000493191.1:n.*509T=
ENST00000641388.1:n.597+30T=
ENST00000641393.1:c.900+30T= ENSP00000493197.1:n.900+30T=
ENST00000641397.1:c.*235+30T= ENSP00000493406.1:n.*235+30T=
ENST00000641413.1:c.275+30T=
ENST00000641434.1:c.1350+30T= ENSP00000493279.1:n.1350+30T=
ENST00000641464.1:c.*583+30T= ENSP00000493438.1:n.*583+30T=
ENST00000641482.1:c.*265T= ENSP00000493277.1:n.*265T=
ENST00000641508.1:c.*583+30T= ENSP00000493209.1:n.*583+30T=
ENST00000641509.1:c.1035+30T= ENSP00000493459.1:n.1035+30T=
ENST00000641590.1:c.*265T= ENSP00000493132.1:n.*265T=
ENST00000641658.1:c.*515+30T= ENSP00000492987.1:n.*515+30T=
ENST00000641686.2:c.1350+30T= MANE Select ENSP00000493218.2:n.1350+30T=
ENST00000641690.1:c.1149+30T= ENSP00000492966.1:n.1149+30T=
ENST00000641742.1:c.*515+30T= ENSP00000493315.1:n.*515+30T=
ENST00000641748.1:c.1350+30T= ENSP00000493330.1:n.1350+30T=
ENST00000641753.1:c.1177+30T=
ENST00000641774.1:c.*602+30T= ENSP00000492960.1:n.*602+30T=
ENST00000641830.1:c.612T=
ENST00000641843.1:c.*411+30T= ENSP00000493174.1:n.*411+30T=
ENST00000641869.1:c.551+30T=
ENST00000641870.1:c.*441T= ENSP00000493044.1:n.*441T=
ENST00000641882.1:c.*515+30T= ENSP00000493301.1:n.*515+30T=
ENST00000641928.1:c.*479+30T= ENSP00000493418.1:n.*479+30T=
ENST00000641949.1:c.554-658T= ENSP00000492891.1:n.554-658T=
ENST00000642012.1:n.1214+30T=
ENST00000642034.1:c.*235+30T= ENSP00000493285.1:n.*235+30T=
ENST00000642042.1:c.*12T= ENSP00000493260.1:n.*12T=
ENST00000642078.1:c.*411+30T= ENSP00000492885.1:n.*411+30T=
ENST00000296468.7:c.1350+30T= ENSP00000296468.3:n.1350+30T=
ENST00000504126.1:n.408T=
ENST00000513559.5:c.1215+30T= ENSP00000425000.1:n.1215+30T=
ENST00000515130.5:n.1692+30T=
NM_152778.2:c.1350+30T= NP_689991.1:n.1350+30T=
XM_005262893.1:c.1350+30T= XP_005262950.1:n.1350+30T=
XM_005262896.1:c.1203+30T= XP_005262953.1:n.1203+30T=
XM_005262897.1:c.1149+30T= XP_005262954.1:n.1149+30T=
XM_005262898.2:c.*265T= XP_005262955.1:n.*265T=
XM_011531830.1:c.1236+30T= XP_011530132.1:n.1236+30T=
XM_011531831.1:c.1035+30T= XP_011530133.1:n.1035+30T=
XM_011531832.1:c.*265T= XP_011530134.1:n.*265T=
XR_938717.1:n.1457T=
NM_001363520.1:c.1149+30T= NP_001350449.1:n.1149+30T=
NM_001363521.1:c.1035+30T= NP_001350450.1:n.1035+30T=
XM_005262898.3:c.*265T= XP_005262955.1:n.*265T=
XM_017007989.1:c.*265T= XP_016863478.1:n.*265T=
XM_024453981.1:c.1215+30T= XP_024309749.1:n.1215+30T=
XM_024453982.1:c.1101+30T= XP_024309750.1:n.1101+30T=
XM_024453983.1:c.900+30T= XP_024309751.1:n.900+30T=
XR_001741194.1:n.1323+30T=
XR_001741195.1:n.1209+30T=
XR_001741196.1:n.1122+30T=
XR_001741197.1:n.1312T=
XR_001741198.2:n.1208T=
XR_001741199.1:n.1178+30T=
XR_938717.2:n.1457T=
NM_001363520.2:c.1149+30T= NP_001350449.1:n.1149+30T=
NM_001363521.2:c.1035+30T= NP_001350450.1:n.1035+30T=
NM_001371590.1:c.1215+30T= NP_001358519.1:n.1215+30T=
NM_001371591.1:c.1359+21T= NP_001358520.1:n.1359+21T=
NM_001371592.1:c.1356+30T= NP_001358521.1:n.1356+30T=
NM_001371593.1:c.1236+30T= NP_001358522.1:n.1236+30T=
NM_001371594.1:c.1203+30T= NP_001358523.1:n.1203+30T=
NM_001371595.1:c.1068+30T= NP_001358524.1:n.1068+30T=
NM_001371596.2:c.1350+30T= MANE Select NP_001358525.1:n.1350+30T=
NM_152778.3:c.1350+30T= NP_689991.1:n.1350+30T=
NM_152778.4:c.1350+30T= NP_689991.1:n.1350+30T=