Canonical Allele Identifier: CA1492804598
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921953G= , CM000666.2:g.127921953G= GRCh38
NC_000004.11:g.128843108G= , CM000666.1:g.128843108G= GRCh37
NC_000004.10:g.129062558G= NCBI36
NG_008657.1:g.49032C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1009C= ENSP00000296468.3:p.Arg337=
ENST00000509826.2:c.*242C= ENSP00000421176.2:n.*242C=
ENST00000513559.6:c.727C= ENSP00000425000.2:p.Arg243=
ENST00000515130.6:c.864-182C= ENSP00000493056.1:n.864-182C=
ENST00000641025.1:c.999-182C= ENSP00000493346.1:n.999-182C=
ENST00000641092.1:c.798-182C= ENSP00000493392.1:n.798-182C=
ENST00000641133.1:c.*323C= ENSP00000493192.1:n.*323C=
ENST00000641146.1:n.875C=
ENST00000641147.1:c.559C= ENSP00000493133.1:p.Arg187=
ENST00000641178.1:c.874C= ENSP00000492989.1:p.Arg292=
ENST00000641186.1:c.895C= ENSP00000493347.1:p.Arg299=
ENST00000641228.1:c.798-182C= ENSP00000493194.1:n.798-182C=
ENST00000641332.1:c.*164-182C= ENSP00000493397.1:n.*164-182C=
ENST00000641340.1:c.*232-182C= ENSP00000493191.1:n.*232-182C=
ENST00000641388.1:n.350-182C=
ENST00000641393.1:c.559C= ENSP00000493197.1:p.Arg187=
ENST00000641397.1:c.684-182C= ENSP00000493406.1:n.684-182C=
ENST00000641413.1:c.28-182C=
ENST00000641434.1:c.1009C= ENSP00000493279.1:p.Arg337=
ENST00000641464.1:c.*242C= ENSP00000493438.1:n.*242C=
ENST00000641482.1:c.999-182C= ENSP00000493277.1:n.999-182C=
ENST00000641508.1:c.*242C= ENSP00000493209.1:n.*242C=
ENST00000641509.1:c.694C= ENSP00000493459.1:p.Arg232=
ENST00000641538.1:c.720C=
ENST00000641590.1:c.885-182C= ENSP00000493132.1:n.885-182C=
ENST00000641658.1:c.*174C= ENSP00000492987.1:n.*174C=
ENST00000641686.2:c.1009C= MANE Select ENSP00000493218.2:p.Arg337=
ENST00000641690.1:c.808C= ENSP00000492966.1:p.Arg270=
ENST00000641742.1:c.*174C= ENSP00000493315.1:n.*174C=
ENST00000641748.1:c.1009C= ENSP00000493330.1:p.Arg337=
ENST00000641753.1:c.836C=
ENST00000641774.1:c.*261C= ENSP00000492960.1:n.*261C=
ENST00000641830.1:c.335-182C=
ENST00000641843.1:c.*164-182C= ENSP00000493174.1:n.*164-182C=
ENST00000641869.1:c.304-182C=
ENST00000641870.1:c.*164-182C= ENSP00000493044.1:n.*164-182C=
ENST00000641882.1:c.*174C= ENSP00000493301.1:n.*174C=
ENST00000641928.1:c.*232-182C= ENSP00000493418.1:n.*232-182C=
ENST00000641949.1:c.554-1117C= ENSP00000492891.1:n.554-1117C=
ENST00000642012.1:n.873C=
ENST00000642034.1:c.885-182C= ENSP00000493285.1:n.885-182C=
ENST00000642042.1:c.1009C= ENSP00000493260.1:p.Arg337=
ENST00000642078.1:c.*164-182C= ENSP00000492885.1:n.*164-182C=
ENST00000296468.7:c.1009C= ENSP00000296468.3:p.Arg337=
ENST00000504126.1:n.37C=
ENST00000505284.5:n.894-182C=
ENST00000509826.1:c.*242C= ENSP00000421176.1:n.*242C=
ENST00000513559.5:c.874C= ENSP00000425000.1:p.Arg292=
ENST00000515130.5:n.1445-182C=
NM_152778.2:c.1009C= NP_689991.1:p.Arg337=
XM_005262893.1:c.1009C= XP_005262950.1:p.Arg337=
XM_005262896.1:c.862C= XP_005262953.1:p.Arg288=
XM_005262897.1:c.808C= XP_005262954.1:p.Arg270=
XM_005262898.2:c.999-182C= XP_005262955.1:n.999-182C=
XM_011531830.1:c.895C= XP_011530132.1:p.Arg299=
XM_011531831.1:c.694C= XP_011530133.1:p.Arg232=
XM_011531832.1:c.885-182C= XP_011530134.1:n.885-182C=
XR_938717.1:n.1086C=
NM_001363520.1:c.808C= NP_001350449.1:p.Arg270=
NM_001363521.1:c.694C= NP_001350450.1:p.Arg232=
XM_005262898.3:c.999-182C= XP_005262955.1:n.999-182C=
XM_017007989.1:c.798-182C= XP_016863478.1:n.798-182C=
XM_024453981.1:c.874C= XP_024309749.1:p.Arg292=
XM_024453982.1:c.760C= XP_024309750.1:p.Arg254=
XM_024453983.1:c.559C= XP_024309751.1:p.Arg187=
XR_001741194.1:n.1076-182C=
XR_001741195.1:n.962-182C=
XR_001741196.1:n.875-182C=
XR_001741197.1:n.941C=
XR_001741198.2:n.931-182C=
XR_001741199.1:n.931-182C=
XR_938717.2:n.1086C=
NM_001363520.2:c.808C= NP_001350449.1:p.Arg270=
NM_001363521.2:c.694C= NP_001350450.1:p.Arg232=
NM_001371590.1:c.874C= NP_001358519.1:p.Arg292=
NM_001371591.1:c.1009C= NP_001358520.1:p.Arg337=
NM_001371592.1:c.1015C= NP_001358521.1:p.Arg339=
NM_001371593.1:c.895C= NP_001358522.1:p.Arg299=
NM_001371594.1:c.862C= NP_001358523.1:p.Arg288=
NM_001371595.1:c.727C= NP_001358524.1:p.Arg243=
NM_001371596.2:c.1009C= MANE Select NP_001358525.1:p.Arg337=
NM_152778.3:c.1009C= NP_689991.1:p.Arg337=
NM_152778.4:c.1009C= NP_689991.1:p.Arg337=