Canonical Allele Identifier: CA1492804578
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921937C= , CM000666.2:g.127921937C= GRCh38
NC_000004.11:g.128843092C= , CM000666.1:g.128843092C= GRCh37
NC_000004.10:g.129062542C= NCBI36
NG_008657.1:g.49048G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1025G= ENSP00000296468.3:p.Gly342=
ENST00000509826.2:c.*258G= ENSP00000421176.2:n.*258G=
ENST00000513559.6:c.743G= ENSP00000425000.2:p.Gly248=
ENST00000515130.6:c.864-166G= ENSP00000493056.1:n.864-166G=
ENST00000641025.1:c.999-166G= ENSP00000493346.1:n.999-166G=
ENST00000641092.1:c.798-166G= ENSP00000493392.1:n.798-166G=
ENST00000641133.1:c.*339G= ENSP00000493192.1:n.*339G=
ENST00000641146.1:n.891G=
ENST00000641147.1:c.575G= ENSP00000493133.1:p.Gly192=
ENST00000641178.1:c.890G= ENSP00000492989.1:p.Gly297=
ENST00000641186.1:c.911G= ENSP00000493347.1:p.Gly304=
ENST00000641228.1:c.798-166G= ENSP00000493194.1:n.798-166G=
ENST00000641332.1:c.*164-166G= ENSP00000493397.1:n.*164-166G=
ENST00000641340.1:c.*232-166G= ENSP00000493191.1:n.*232-166G=
ENST00000641388.1:n.350-166G=
ENST00000641393.1:c.575G= ENSP00000493197.1:p.Gly192=
ENST00000641397.1:c.684-166G= ENSP00000493406.1:n.684-166G=
ENST00000641413.1:c.28-166G=
ENST00000641434.1:c.1025G= ENSP00000493279.1:p.Gly342=
ENST00000641464.1:c.*258G= ENSP00000493438.1:n.*258G=
ENST00000641482.1:c.999-166G= ENSP00000493277.1:n.999-166G=
ENST00000641508.1:c.*258G= ENSP00000493209.1:n.*258G=
ENST00000641509.1:c.710G= ENSP00000493459.1:p.Gly237=
ENST00000641538.1:c.736G=
ENST00000641590.1:c.885-166G= ENSP00000493132.1:n.885-166G=
ENST00000641658.1:c.*190G= ENSP00000492987.1:n.*190G=
ENST00000641686.2:c.1025G= MANE Select ENSP00000493218.2:p.Gly342=
ENST00000641690.1:c.824G= ENSP00000492966.1:p.Gly275=
ENST00000641742.1:c.*190G= ENSP00000493315.1:n.*190G=
ENST00000641748.1:c.1025G= ENSP00000493330.1:p.Gly342=
ENST00000641753.1:c.852G=
ENST00000641774.1:c.*277G= ENSP00000492960.1:n.*277G=
ENST00000641830.1:c.335-166G=
ENST00000641843.1:c.*164-166G= ENSP00000493174.1:n.*164-166G=
ENST00000641869.1:c.304-166G=
ENST00000641870.1:c.*164-166G= ENSP00000493044.1:n.*164-166G=
ENST00000641882.1:c.*190G= ENSP00000493301.1:n.*190G=
ENST00000641928.1:c.*232-166G= ENSP00000493418.1:n.*232-166G=
ENST00000641949.1:c.554-1101G= ENSP00000492891.1:n.554-1101G=
ENST00000642012.1:n.889G=
ENST00000642034.1:c.885-166G= ENSP00000493285.1:n.885-166G=
ENST00000642042.1:c.1025G= ENSP00000493260.1:p.Gly342=
ENST00000642078.1:c.*164-166G= ENSP00000492885.1:n.*164-166G=
ENST00000296468.7:c.1025G= ENSP00000296468.3:p.Gly342=
ENST00000504126.1:n.53G=
ENST00000505284.5:n.894-166G=
ENST00000509826.1:c.*258G= ENSP00000421176.1:n.*258G=
ENST00000513559.5:c.890G= ENSP00000425000.1:p.Gly297=
ENST00000515130.5:n.1445-166G=
NM_152778.2:c.1025G= NP_689991.1:p.Gly342=
XM_005262893.1:c.1025G= XP_005262950.1:p.Gly342=
XM_005262896.1:c.878G= XP_005262953.1:p.Gly293=
XM_005262897.1:c.824G= XP_005262954.1:p.Gly275=
XM_005262898.2:c.999-166G= XP_005262955.1:n.999-166G=
XM_011531830.1:c.911G= XP_011530132.1:p.Gly304=
XM_011531831.1:c.710G= XP_011530133.1:p.Gly237=
XM_011531832.1:c.885-166G= XP_011530134.1:n.885-166G=
XR_938717.1:n.1102G=
NM_001363520.1:c.824G= NP_001350449.1:p.Gly275=
NM_001363521.1:c.710G= NP_001350450.1:p.Gly237=
XM_005262898.3:c.999-166G= XP_005262955.1:n.999-166G=
XM_017007989.1:c.798-166G= XP_016863478.1:n.798-166G=
XM_024453981.1:c.890G= XP_024309749.1:p.Gly297=
XM_024453982.1:c.776G= XP_024309750.1:p.Gly259=
XM_024453983.1:c.575G= XP_024309751.1:p.Gly192=
XR_001741194.1:n.1076-166G=
XR_001741195.1:n.962-166G=
XR_001741196.1:n.875-166G=
XR_001741197.1:n.957G=
XR_001741198.2:n.931-166G=
XR_001741199.1:n.931-166G=
XR_938717.2:n.1102G=
NM_001363520.2:c.824G= NP_001350449.1:p.Gly275=
NM_001363521.2:c.710G= NP_001350450.1:p.Gly237=
NM_001371590.1:c.890G= NP_001358519.1:p.Gly297=
NM_001371591.1:c.1025G= NP_001358520.1:p.Gly342=
NM_001371592.1:c.1031G= NP_001358521.1:p.Gly344=
NM_001371593.1:c.911G= NP_001358522.1:p.Gly304=
NM_001371594.1:c.878G= NP_001358523.1:p.Gly293=
NM_001371595.1:c.743G= NP_001358524.1:p.Gly248=
NM_001371596.2:c.1025G= MANE Select NP_001358525.1:p.Gly342=
NM_152778.3:c.1025G= NP_689991.1:p.Gly342=
NM_152778.4:c.1025G= NP_689991.1:p.Gly342=