Canonical Allele Identifier: CA1187870660

Gene: AKNAD1 GPSM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876918T= , CM000663.2:g.108876918T=	GRCh38
NC_000001.10:g.109419540T= , CM000663.1:g.109419540T=	GRCh37
NC_000001.9:g.109221063T=	NCBI36
NG_028108.1:g.4938T=
NG_028108.2:g.6569T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357393.6:c.1-27342A= (AKNAD1)	ENSP00000349968.6:n.1-27342A=
ENST00000357393.5:c.115-27342A=	ENSP00000349968.5:n.115-27342A=
ENST00000406462.6:c.-559T= (GPSM2)	ENSP00000385510.1:n.-559T=
XM_005270787.2:c.-327T= (GPSM2)	XP_005270844.1:n.-327T=
XM_006710589.1:c.-312T= (GPSM2)	XP_006710652.1:n.-312T=
XM_011541301.1:c.-559T= (GPSM2)	XP_011539603.1:n.-559T=
XM_011541303.1:c.-559T= (GPSM2)	XP_011539605.1:n.-559T=
XM_006710589.3:c.-312T= (GPSM2)	XP_006710652.1:n.-312T=
XM_011541301.2:c.-559T= (GPSM2)	XP_011539603.1:n.-559T=
XM_011541302.3:c.-803T= (GPSM2)	XP_011539604.1:n.-803T=
XM_011541303.3:c.-559T= (GPSM2)	XP_011539605.1:n.-559T=
XM_017001097.2:c.-709T= (GPSM2)	XP_016856586.1:n.-709T=
XM_017001098.2:c.-477T= (GPSM2)	XP_016856587.1:n.-477T=