Canonical Allele Identifier: CA105670523
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1183498
ClinVar RCV Id: RCV001541355
dbSNP Id: rs76719935

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921414G>T , CM000666.2:g.127921414G>T GRCh38
NC_000004.11:g.128842569G>T , CM000666.1:g.128842569G>T GRCh37
NC_000004.10:g.129062019G>T NCBI36
NG_008657.1:g.49571C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1350+110C>A ENSP00000296468.3:n.1350+110C>A
ENST00000509826.2:c.*671+110C>A ENSP00000421176.2:n.*671+110C>A
ENST00000513559.6:c.1068+110C>A ENSP00000425000.2:n.1068+110C>A
ENST00000515130.6:c.*235+110C>A ENSP00000493056.1:n.*235+110C>A
ENST00000641025.1:c.*235+110C>A ENSP00000493346.1:n.*235+110C>A
ENST00000641092.1:c.*235+110C>A ENSP00000493392.1:n.*235+110C>A
ENST00000641133.1:c.*774C>A ENSP00000493192.1:n.*774C>A
ENST00000641146.1:n.1326C>A
ENST00000641147.1:c.900+110C>A ENSP00000493133.1:n.900+110C>A
ENST00000641178.1:c.1215+110C>A ENSP00000492989.1:n.1215+110C>A
ENST00000641186.1:c.1236+110C>A ENSP00000493347.1:n.1236+110C>A
ENST00000641228.1:c.*345C>A ENSP00000493194.1:n.*345C>A
ENST00000641332.1:c.*411+110C>A ENSP00000493397.1:n.*411+110C>A
ENST00000641340.1:c.*589C>A ENSP00000493191.1:n.*589C>A
ENST00000641388.1:n.597+110C>A
ENST00000641393.1:c.900+110C>A ENSP00000493197.1:n.900+110C>A
ENST00000641397.1:c.*235+110C>A ENSP00000493406.1:n.*235+110C>A
ENST00000641413.1:c.275+110C>A
ENST00000641434.1:c.1350+110C>A ENSP00000493279.1:n.1350+110C>A
ENST00000641464.1:c.*583+110C>A ENSP00000493438.1:n.*583+110C>A
ENST00000641482.1:c.*345C>A ENSP00000493277.1:n.*345C>A
ENST00000641508.1:c.*583+110C>A ENSP00000493209.1:n.*583+110C>A
ENST00000641509.1:c.1035+110C>A ENSP00000493459.1:n.1035+110C>A
ENST00000641590.1:c.*345C>A ENSP00000493132.1:n.*345C>A
ENST00000641658.1:c.*515+110C>A ENSP00000492987.1:n.*515+110C>A
ENST00000641686.2:c.1350+110C>A MANE Select ENSP00000493218.2:n.1350+110C>A
ENST00000641690.1:c.1149+110C>A ENSP00000492966.1:n.1149+110C>A
ENST00000641742.1:c.*515+110C>A ENSP00000493315.1:n.*515+110C>A
ENST00000641748.1:c.1350+110C>A ENSP00000493330.1:n.1350+110C>A
ENST00000641753.1:c.1177+110C>A
ENST00000641774.1:c.*602+110C>A ENSP00000492960.1:n.*602+110C>A
ENST00000641843.1:c.*411+110C>A ENSP00000493174.1:n.*411+110C>A
ENST00000641869.1:c.551+110C>A
ENST00000641870.1:c.*521C>A ENSP00000493044.1:n.*521C>A
ENST00000641882.1:c.*515+110C>A ENSP00000493301.1:n.*515+110C>A
ENST00000641928.1:c.*479+110C>A ENSP00000493418.1:n.*479+110C>A
ENST00000641949.1:c.554-578C>A ENSP00000492891.1:n.554-578C>A
ENST00000642012.1:n.1214+110C>A
ENST00000642034.1:c.*235+110C>A ENSP00000493285.1:n.*235+110C>A
ENST00000642042.1:c.*92C>A ENSP00000493260.1:n.*92C>A
ENST00000642078.1:c.*411+110C>A ENSP00000492885.1:n.*411+110C>A
ENST00000296468.7:c.1350+110C>A ENSP00000296468.3:n.1350+110C>A
ENST00000504126.1:n.488C>A
ENST00000513559.5:c.1215+110C>A ENSP00000425000.1:n.1215+110C>A
ENST00000515130.5:n.1692+110C>A
NM_152778.2:c.1350+110C>A NP_689991.1:n.1350+110C>A
XM_005262893.1:c.1350+110C>A XP_005262950.1:n.1350+110C>A
XM_005262896.1:c.1203+110C>A XP_005262953.1:n.1203+110C>A
XM_005262897.1:c.1149+110C>A XP_005262954.1:n.1149+110C>A
XM_005262898.2:c.*345C>A XP_005262955.1:n.*345C>A
XM_011531830.1:c.1236+110C>A XP_011530132.1:n.1236+110C>A
XM_011531831.1:c.1035+110C>A XP_011530133.1:n.1035+110C>A
XM_011531832.1:c.*345C>A XP_011530134.1:n.*345C>A
XR_938717.1:n.1537C>A
NM_001363520.1:c.1149+110C>A NP_001350449.1:n.1149+110C>A
NM_001363521.1:c.1035+110C>A NP_001350450.1:n.1035+110C>A
XM_005262898.3:c.*345C>A XP_005262955.1:n.*345C>A
XM_017007989.1:c.*345C>A XP_016863478.1:n.*345C>A
XM_024453981.1:c.1215+110C>A XP_024309749.1:n.1215+110C>A
XM_024453982.1:c.1101+110C>A XP_024309750.1:n.1101+110C>A
XM_024453983.1:c.900+110C>A XP_024309751.1:n.900+110C>A
XR_001741194.1:n.1323+110C>A
XR_001741195.1:n.1209+110C>A
XR_001741196.1:n.1122+110C>A
XR_001741197.1:n.1392C>A
XR_001741198.2:n.1288C>A
XR_001741199.1:n.1178+110C>A
XR_938717.2:n.1537C>A
NM_001363520.2:c.1149+110C>A NP_001350449.1:n.1149+110C>A
NM_001363521.2:c.1035+110C>A NP_001350450.1:n.1035+110C>A
NM_001371590.1:c.1215+110C>A NP_001358519.1:n.1215+110C>A
NM_001371591.1:c.1359+101C>A NP_001358520.1:n.1359+101C>A
NM_001371592.1:c.1356+110C>A NP_001358521.1:n.1356+110C>A
NM_001371593.1:c.1236+110C>A NP_001358522.1:n.1236+110C>A
NM_001371594.1:c.1203+110C>A NP_001358523.1:n.1203+110C>A
NM_001371595.1:c.1068+110C>A NP_001358524.1:n.1068+110C>A
NM_001371596.2:c.1350+110C>A MANE Select NP_001358525.1:n.1350+110C>A
NM_152778.3:c.1350+110C>A NP_689991.1:n.1350+110C>A
NM_152778.4:c.1350+110C>A NP_689991.1:n.1350+110C>A