Canonical Allele Identifier: CA2646882460

Gene: AKNAD1 GPSM2

Linked Data

• gnomAD v4: 1-108876908-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876908C>A , CM000663.2:g.108876908C>A	GRCh38
NC_000001.10:g.109419530C>A , CM000663.1:g.109419530C>A	GRCh37
NC_000001.9:g.109221053C>A	NCBI36
NG_028108.1:g.4928C>A
NG_028108.2:g.6559C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357393.6:c.1-27332G>T (AKNAD1)	ENSP00000349968.6:n.1-27332G>T
ENST00000357393.5:c.115-27332G>T	ENSP00000349968.5:n.115-27332G>T
ENST00000406462.6:c.-569C>A (GPSM2)	ENSP00000385510.1:n.-569C>A
XM_005270787.2:c.-337C>A (GPSM2)	XP_005270844.1:n.-337C>A
XM_006710589.1:c.-322C>A (GPSM2)	XP_006710652.1:n.-322C>A
XM_011541301.1:c.-569C>A (GPSM2)	XP_011539603.1:n.-569C>A
XM_011541303.1:c.-569C>A (GPSM2)	XP_011539605.1:n.-569C>A
XM_006710589.3:c.-322C>A (GPSM2)	XP_006710652.1:n.-322C>A
XM_011541301.2:c.-569C>A (GPSM2)	XP_011539603.1:n.-569C>A
XM_011541302.3:c.-813C>A (GPSM2)	XP_011539604.1:n.-813C>A
XM_011541303.3:c.-569C>A (GPSM2)	XP_011539605.1:n.-569C>A
XM_017001097.2:c.-719C>A (GPSM2)	XP_016856586.1:n.-719C>A
XM_017001098.2:c.-487C>A (GPSM2)	XP_016856587.1:n.-487C>A