Canonical Allele Identifier: CA2580071509
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012597
ClinVar RCV Id: RCV002843233

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921538del , CM000666.2:g.127921538del GRCh38
NC_000004.11:g.128842693del , CM000666.1:g.128842693del GRCh37
NC_000004.10:g.129062143del NCBI36
NG_008657.1:g.49448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1337del ENSP00000296468.3:p.Gly446AspfsTer12
ENST00000509826.2:c.*658del ENSP00000421176.2:n.*658del
ENST00000513559.6:c.1055del ENSP00000425000.2:p.Gly352AspfsTer12
ENST00000515130.6:c.*222del ENSP00000493056.1:n.*222del
ENST00000641025.1:c.*222del ENSP00000493346.1:n.*222del
ENST00000641092.1:c.*222del ENSP00000493392.1:n.*222del
ENST00000641133.1:c.*651del ENSP00000493192.1:n.*651del
ENST00000641146.1:n.1203del
ENST00000641147.1:c.887del ENSP00000493133.1:p.Gly296AspfsTer12
ENST00000641178.1:c.1202del ENSP00000492989.1:p.Gly401AspfsTer12
ENST00000641186.1:c.1223del ENSP00000493347.1:p.Gly408AspfsTer12
ENST00000641228.1:c.*222del ENSP00000493194.1:n.*222del
ENST00000641332.1:c.*398del ENSP00000493397.1:n.*398del
ENST00000641340.1:c.*466del ENSP00000493191.1:n.*466del
ENST00000641388.1:n.584del
ENST00000641393.1:c.887del ENSP00000493197.1:p.Gly296AspfsTer12
ENST00000641397.1:c.*222del ENSP00000493406.1:n.*222del
ENST00000641413.1:c.262del
ENST00000641434.1:c.1337del ENSP00000493279.1:p.Gly446AspfsTer12
ENST00000641464.1:c.*570del ENSP00000493438.1:n.*570del
ENST00000641482.1:c.*222del ENSP00000493277.1:n.*222del
ENST00000641508.1:c.*570del ENSP00000493209.1:n.*570del
ENST00000641509.1:c.1022del ENSP00000493459.1:p.Gly341AspfsTer12
ENST00000641590.1:c.*222del ENSP00000493132.1:n.*222del
ENST00000641658.1:c.*502del ENSP00000492987.1:n.*502del
ENST00000641686.2:c.1337del MANE Select ENSP00000493218.2:p.Gly446AspfsTer12
ENST00000641690.1:c.1136del ENSP00000492966.1:p.Gly379AspfsTer12
ENST00000641742.1:c.*502del ENSP00000493315.1:n.*502del
ENST00000641748.1:c.1337del ENSP00000493330.1:p.Gly446AspfsTer12
ENST00000641753.1:c.1164del
ENST00000641774.1:c.*589del ENSP00000492960.1:n.*589del
ENST00000641830.1:c.569del
ENST00000641843.1:c.*398del ENSP00000493174.1:n.*398del
ENST00000641869.1:c.538del
ENST00000641870.1:c.*398del ENSP00000493044.1:n.*398del
ENST00000641882.1:c.*502del ENSP00000493301.1:n.*502del
ENST00000641928.1:c.*466del ENSP00000493418.1:n.*466del
ENST00000641949.1:c.554-701del ENSP00000492891.1:n.554-701del
ENST00000642012.1:n.1201del
ENST00000642034.1:c.*222del ENSP00000493285.1:n.*222del
ENST00000642042.1:c.1337del ENSP00000493260.1:p.Gly446AspfsTer6
ENST00000642078.1:c.*398del ENSP00000492885.1:n.*398del
ENST00000296468.7:c.1337del ENSP00000296468.3:p.Gly446AspfsTer12
ENST00000504126.1:n.365del
ENST00000513559.5:c.1202del ENSP00000425000.1:p.Gly401AspfsTer12
ENST00000515130.5:n.1679del
NM_152778.2:c.1337del NP_689991.1:p.Gly446AspfsTer12
XM_005262893.1:c.1337del XP_005262950.1:p.Gly446AspfsTer12
XM_005262896.1:c.1190del XP_005262953.1:p.Gly397AspfsTer12
XM_005262897.1:c.1136del XP_005262954.1:p.Gly379AspfsTer12
XM_005262898.2:c.*222del XP_005262955.1:n.*222del
XM_011531830.1:c.1223del XP_011530132.1:p.Gly408AspfsTer12
XM_011531831.1:c.1022del XP_011530133.1:p.Gly341AspfsTer12
XM_011531832.1:c.*222del XP_011530134.1:n.*222del
XR_938717.1:n.1414del
NM_001363520.1:c.1136del NP_001350449.1:p.Gly379AspfsTer12
NM_001363521.1:c.1022del NP_001350450.1:p.Gly341AspfsTer12
XM_005262898.3:c.*222del XP_005262955.1:n.*222del
XM_017007989.1:c.*222del XP_016863478.1:n.*222del
XM_024453981.1:c.1202del XP_024309749.1:p.Gly401AspfsTer12
XM_024453982.1:c.1088del XP_024309750.1:p.Gly363AspfsTer12
XM_024453983.1:c.887del XP_024309751.1:p.Gly296AspfsTer12
XR_001741194.1:n.1310del
XR_001741195.1:n.1196del
XR_001741196.1:n.1109del
XR_001741197.1:n.1269del
XR_001741198.2:n.1165del
XR_001741199.1:n.1165del
XR_938717.2:n.1414del
NM_001363520.2:c.1136del NP_001350449.1:p.Gly379AspfsTer12
NM_001363521.2:c.1022del NP_001350450.1:p.Gly341AspfsTer12
NM_001371590.1:c.1202del NP_001358519.1:p.Gly401AspfsTer12
NM_001371591.1:c.1337del NP_001358520.1:p.Gly446AspfsTer6
NM_001371592.1:c.1343del NP_001358521.1:p.Gly448AspfsTer12
NM_001371593.1:c.1223del NP_001358522.1:p.Gly408AspfsTer12
NM_001371594.1:c.1190del NP_001358523.1:p.Gly397AspfsTer12
NM_001371595.1:c.1055del NP_001358524.1:p.Gly352AspfsTer12
NM_001371596.2:c.1337del MANE Select NP_001358525.1:p.Gly446AspfsTer12
NM_152778.3:c.1337del NP_689991.1:p.Gly446AspfsTer12
NM_152778.4:c.1337del NP_689991.1:p.Gly446AspfsTer12