Canonical Allele Identifier: CA28585751

Gene: AKNAD1 GPSM2

Linked Data

• dbSNP Id: rs936142833
• MyVariant Identifiers: chr1:g.109419593G>A (hg19) ; chr1:g.108876971G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876971G>A , CM000663.2:g.108876971G>A	GRCh38
NC_000001.10:g.109419593G>A , CM000663.1:g.109419593G>A	GRCh37
NC_000001.9:g.109221116G>A	NCBI36
NG_028108.1:g.4991G>A
NG_028108.2:g.6622G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357393.6:c.1-27395C>T (AKNAD1)	ENSP00000349968.6:n.1-27395C>T
ENST00000675829.1:n.12G>A (GPSM2)
ENST00000357393.5:c.115-27395C>T	ENSP00000349968.5:n.115-27395C>T
ENST00000406462.6:c.-506G>A (GPSM2)	ENSP00000385510.1:n.-506G>A
XM_005270787.2:c.-274G>A (GPSM2)	XP_005270844.1:n.-274G>A
XM_006710589.1:c.-259G>A (GPSM2)	XP_006710652.1:n.-259G>A
XM_011541301.1:c.-506G>A (GPSM2)	XP_011539603.1:n.-506G>A
XM_011541303.1:c.-506G>A (GPSM2)	XP_011539605.1:n.-506G>A
XM_006710589.3:c.-259G>A (GPSM2)	XP_006710652.1:n.-259G>A
XM_011541301.2:c.-506G>A (GPSM2)	XP_011539603.1:n.-506G>A
XM_011541302.3:c.-750G>A (GPSM2)	XP_011539604.1:n.-750G>A
XM_011541303.3:c.-506G>A (GPSM2)	XP_011539605.1:n.-506G>A
XM_017001097.2:c.-656G>A (GPSM2)	XP_016856586.1:n.-656G>A
XM_017001098.2:c.-424G>A (GPSM2)	XP_016856587.1:n.-424G>A