Canonical Allele Identifier: CA1187870683

Gene: AKNAD1 GPSM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876948C= , CM000663.2:g.108876948C=	GRCh38
NC_000001.10:g.109419570C= , CM000663.1:g.109419570C=	GRCh37
NC_000001.9:g.109221093C=	NCBI36
NG_028108.1:g.4968C=
NG_028108.2:g.6599C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357393.6:c.1-27372G= (AKNAD1)	ENSP00000349968.6:n.1-27372G=
ENST00000357393.5:c.115-27372G=	ENSP00000349968.5:n.115-27372G=
ENST00000406462.6:c.-529C= (GPSM2)	ENSP00000385510.1:n.-529C=
XM_005270787.2:c.-297C= (GPSM2)	XP_005270844.1:n.-297C=
XM_006710589.1:c.-282C= (GPSM2)	XP_006710652.1:n.-282C=
XM_011541301.1:c.-529C= (GPSM2)	XP_011539603.1:n.-529C=
XM_011541303.1:c.-529C= (GPSM2)	XP_011539605.1:n.-529C=
XM_006710589.3:c.-282C= (GPSM2)	XP_006710652.1:n.-282C=
XM_011541301.2:c.-529C= (GPSM2)	XP_011539603.1:n.-529C=
XM_011541302.3:c.-773C= (GPSM2)	XP_011539604.1:n.-773C=
XM_011541303.3:c.-529C= (GPSM2)	XP_011539605.1:n.-529C=
XM_017001097.2:c.-679C= (GPSM2)	XP_016856586.1:n.-679C=
XM_017001098.2:c.-447C= (GPSM2)	XP_016856587.1:n.-447C=