Canonical Allele Identifier: CA1187870668

Gene: AKNAD1 GPSM2

Linked Data

• dbSNP Id: rs1665638304

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876929G>A , CM000663.2:g.108876929G>A	GRCh38
NC_000001.10:g.109419551G>A , CM000663.1:g.109419551G>A	GRCh37
NC_000001.9:g.109221074G>A	NCBI36
NG_028108.1:g.4949G>A
NG_028108.2:g.6580G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357393.6:c.1-27353C>T (AKNAD1)	ENSP00000349968.6:n.1-27353C>T
ENST00000357393.5:c.115-27353C>T	ENSP00000349968.5:n.115-27353C>T
ENST00000406462.6:c.-548G>A (GPSM2)	ENSP00000385510.1:n.-548G>A
XM_005270787.2:c.-316G>A (GPSM2)	XP_005270844.1:n.-316G>A
XM_006710589.1:c.-301G>A (GPSM2)	XP_006710652.1:n.-301G>A
XM_011541301.1:c.-548G>A (GPSM2)	XP_011539603.1:n.-548G>A
XM_011541303.1:c.-548G>A (GPSM2)	XP_011539605.1:n.-548G>A
XM_006710589.3:c.-301G>A (GPSM2)	XP_006710652.1:n.-301G>A
XM_011541301.2:c.-548G>A (GPSM2)	XP_011539603.1:n.-548G>A
XM_011541302.3:c.-792G>A (GPSM2)	XP_011539604.1:n.-792G>A
XM_011541303.3:c.-548G>A (GPSM2)	XP_011539605.1:n.-548G>A
XM_017001097.2:c.-698G>A (GPSM2)	XP_016856586.1:n.-698G>A
XM_017001098.2:c.-466G>A (GPSM2)	XP_016856587.1:n.-466G>A