Canonical Allele Identifier: CA1187870661

Gene: AKNAD1 GPSM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876919T= , CM000663.2:g.108876919T=	GRCh38
NC_000001.10:g.109419541T= , CM000663.1:g.109419541T=	GRCh37
NC_000001.9:g.109221064T=	NCBI36
NG_028108.1:g.4939T=
NG_028108.2:g.6570T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357393.6:c.1-27343A= (AKNAD1)	ENSP00000349968.6:n.1-27343A=
ENST00000357393.5:c.115-27343A=	ENSP00000349968.5:n.115-27343A=
ENST00000406462.6:c.-558T= (GPSM2)	ENSP00000385510.1:n.-558T=
XM_005270787.2:c.-326T= (GPSM2)	XP_005270844.1:n.-326T=
XM_006710589.1:c.-311T= (GPSM2)	XP_006710652.1:n.-311T=
XM_011541301.1:c.-558T= (GPSM2)	XP_011539603.1:n.-558T=
XM_011541303.1:c.-558T= (GPSM2)	XP_011539605.1:n.-558T=
XM_006710589.3:c.-311T= (GPSM2)	XP_006710652.1:n.-311T=
XM_011541301.2:c.-558T= (GPSM2)	XP_011539603.1:n.-558T=
XM_011541302.3:c.-802T= (GPSM2)	XP_011539604.1:n.-802T=
XM_011541303.3:c.-558T= (GPSM2)	XP_011539605.1:n.-558T=
XM_017001097.2:c.-708T= (GPSM2)	XP_016856586.1:n.-708T=
XM_017001098.2:c.-476T= (GPSM2)	XP_016856587.1:n.-476T=