Canonical Allele Identifier: CA1492804192

Gene: MFSD8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921675C= , CM000666.2:g.127921675C=	GRCh38
NC_000004.11:g.128842830C= , CM000666.1:g.128842830C=	GRCh37
NC_000004.10:g.129062280C=	NCBI36
NG_008657.1:g.49310G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1199G=	ENSP00000296468.3:p.Gly400=
ENST00000509826.2:c.*520G=	ENSP00000421176.2:n.*520G=
ENST00000513559.6:c.917G=	ENSP00000425000.2:p.Gly306=
ENST00000515130.6:c.*84G=	ENSP00000493056.1:n.*84G=
ENST00000641025.1:c.*84G=	ENSP00000493346.1:n.*84G=
ENST00000641092.1:c.*84G=	ENSP00000493392.1:n.*84G=
ENST00000641133.1:c.*513G=	ENSP00000493192.1:n.*513G=
ENST00000641146.1:n.1065G=
ENST00000641147.1:c.749G=	ENSP00000493133.1:p.Gly250=
ENST00000641178.1:c.1064G=	ENSP00000492989.1:p.Gly355=
ENST00000641186.1:c.1085G=	ENSP00000493347.1:p.Gly362=
ENST00000641228.1:c.*84G=	ENSP00000493194.1:n.*84G=
ENST00000641332.1:c.*260G=	ENSP00000493397.1:n.*260G=
ENST00000641340.1:c.*328G=	ENSP00000493191.1:n.*328G=
ENST00000641388.1:n.446G=
ENST00000641393.1:c.749G=	ENSP00000493197.1:p.Gly250=
ENST00000641397.1:c.*84G=	ENSP00000493406.1:n.*84G=
ENST00000641413.1:c.124G=
ENST00000641434.1:c.1199G=	ENSP00000493279.1:p.Gly400=
ENST00000641464.1:c.*432G=	ENSP00000493438.1:n.*432G=
ENST00000641482.1:c.*84G=	ENSP00000493277.1:n.*84G=
ENST00000641508.1:c.*432G=	ENSP00000493209.1:n.*432G=
ENST00000641509.1:c.884G=	ENSP00000493459.1:p.Gly295=
ENST00000641590.1:c.*84G=	ENSP00000493132.1:n.*84G=
ENST00000641658.1:c.*364G=	ENSP00000492987.1:n.*364G=
ENST00000641686.2:c.1199G= MANE Select	ENSP00000493218.2:p.Gly400=
ENST00000641690.1:c.998G=	ENSP00000492966.1:p.Gly333=
ENST00000641742.1:c.*364G=	ENSP00000493315.1:n.*364G=
ENST00000641748.1:c.1199G=	ENSP00000493330.1:p.Gly400=
ENST00000641753.1:c.1026G=
ENST00000641774.1:c.*451G=	ENSP00000492960.1:n.*451G=
ENST00000641830.1:c.431G=
ENST00000641843.1:c.*260G=	ENSP00000493174.1:n.*260G=
ENST00000641869.1:c.400G=
ENST00000641870.1:c.*260G=	ENSP00000493044.1:n.*260G=
ENST00000641882.1:c.*364G=	ENSP00000493301.1:n.*364G=
ENST00000641928.1:c.*328G=	ENSP00000493418.1:n.*328G=
ENST00000641949.1:c.554-839G=	ENSP00000492891.1:n.554-839G=
ENST00000642012.1:n.1063G=
ENST00000642034.1:c.*84G=	ENSP00000493285.1:n.*84G=
ENST00000642042.1:c.1199G=	ENSP00000493260.1:p.Gly400=
ENST00000642078.1:c.*260G=	ENSP00000492885.1:n.*260G=
ENST00000296468.7:c.1199G=	ENSP00000296468.3:p.Gly400=
ENST00000504126.1:n.227G=
ENST00000513559.5:c.1064G=	ENSP00000425000.1:p.Gly355=
ENST00000515130.5:n.1541G=
NM_152778.2:c.1199G=	NP_689991.1:p.Gly400=
XM_005262893.1:c.1199G=	XP_005262950.1:p.Gly400=
XM_005262896.1:c.1052G=	XP_005262953.1:p.Gly351=
XM_005262897.1:c.998G=	XP_005262954.1:p.Gly333=
XM_005262898.2:c.*84G=	XP_005262955.1:n.*84G=
XM_011531830.1:c.1085G=	XP_011530132.1:p.Gly362=
XM_011531831.1:c.884G=	XP_011530133.1:p.Gly295=
XM_011531832.1:c.*84G=	XP_011530134.1:n.*84G=
XR_938717.1:n.1276G=
NM_001363520.1:c.998G=	NP_001350449.1:p.Gly333=
NM_001363521.1:c.884G=	NP_001350450.1:p.Gly295=
XM_005262898.3:c.*84G=	XP_005262955.1:n.*84G=
XM_017007989.1:c.*84G=	XP_016863478.1:n.*84G=
XM_024453981.1:c.1064G=	XP_024309749.1:p.Gly355=
XM_024453982.1:c.950G=	XP_024309750.1:p.Gly317=
XM_024453983.1:c.749G=	XP_024309751.1:p.Gly250=
XR_001741194.1:n.1172G=
XR_001741195.1:n.1058G=
XR_001741196.1:n.971G=
XR_001741197.1:n.1131G=
XR_001741198.2:n.1027G=
XR_001741199.1:n.1027G=
XR_938717.2:n.1276G=
NM_001363520.2:c.998G=	NP_001350449.1:p.Gly333=
NM_001363521.2:c.884G=	NP_001350450.1:p.Gly295=
NM_001371590.1:c.1064G=	NP_001358519.1:p.Gly355=
NM_001371591.1:c.1199G=	NP_001358520.1:p.Gly400=
NM_001371592.1:c.1205G=	NP_001358521.1:p.Gly402=
NM_001371593.1:c.1085G=	NP_001358522.1:p.Gly362=
NM_001371594.1:c.1052G=	NP_001358523.1:p.Gly351=
NM_001371595.1:c.917G=	NP_001358524.1:p.Gly306=
NM_001371596.2:c.1199G= MANE Select	NP_001358525.1:p.Gly400=
NM_152778.3:c.1199G=	NP_689991.1:p.Gly400=
NM_152778.4:c.1199G=	NP_689991.1:p.Gly400=