Canonical Allele Identifier: CA2646882455

Gene: AKNAD1 GPSM2

Linked Data

• gnomAD v4: 1-108876904-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876904T>C , CM000663.2:g.108876904T>C	GRCh38
NC_000001.10:g.109419526T>C , CM000663.1:g.109419526T>C	GRCh37
NC_000001.9:g.109221049T>C	NCBI36
NG_028108.1:g.4924T>C
NG_028108.2:g.6555T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357393.6:c.1-27328A>G (AKNAD1)	ENSP00000349968.6:n.1-27328A>G
ENST00000357393.5:c.115-27328A>G	ENSP00000349968.5:n.115-27328A>G
ENST00000406462.6:c.-573T>C (GPSM2)	ENSP00000385510.1:n.-573T>C
XM_005270787.2:c.-341T>C (GPSM2)	XP_005270844.1:n.-341T>C
XM_006710589.1:c.-326T>C (GPSM2)	XP_006710652.1:n.-326T>C
XM_011541301.1:c.-573T>C (GPSM2)	XP_011539603.1:n.-573T>C
XM_011541303.1:c.-573T>C (GPSM2)	XP_011539605.1:n.-573T>C
XM_006710589.3:c.-326T>C (GPSM2)	XP_006710652.1:n.-326T>C
XM_011541301.2:c.-573T>C (GPSM2)	XP_011539603.1:n.-573T>C
XM_011541302.3:c.-817T>C (GPSM2)	XP_011539604.1:n.-817T>C
XM_011541303.3:c.-573T>C (GPSM2)	XP_011539605.1:n.-573T>C
XM_017001097.2:c.-723T>C (GPSM2)	XP_016856586.1:n.-723T>C
XM_017001098.2:c.-491T>C (GPSM2)	XP_016856587.1:n.-491T>C