Canonical Allele Identifier: CA2646882507

Gene: AKNAD1 GPSM2

Linked Data

• gnomAD v4: 1-108876984-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108876984C>A , CM000663.2:g.108876984C>A	GRCh38
NC_000001.10:g.109419606C>A , CM000663.1:g.109419606C>A	GRCh37
NC_000001.9:g.109221129C>A	NCBI36
NG_028108.1:g.5004C>A
NG_028108.2:g.6635C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357393.6:c.1-27408G>T (AKNAD1)	ENSP00000349968.6:n.1-27408G>T
ENST00000441735.2:c.-411C>A (GPSM2)	ENSP00000390629.2:n.-411C>A
ENST00000642355.1:c.-493C>A (GPSM2)	ENSP00000496104.1:n.-493C>A
ENST00000645164.2:c.-307C>A (GPSM2)	ENSP00000496756.2:n.-307C>A
ENST00000675776.1:n.3C>A (GPSM2)
ENST00000675829.1:n.25C>A (GPSM2)
ENST00000264126.7:c.-493C>A (GPSM2)	ENSP00000264126.3:n.-493C>A
ENST00000357393.5:c.115-27408G>T	ENSP00000349968.5:n.115-27408G>T
ENST00000406462.6:c.-493C>A (GPSM2)	ENSP00000385510.1:n.-493C>A
ENST00000435987.5:c.-261C>A (GPSM2)	ENSP00000408664.1:n.-261C>A
NM_013296.4:c.-493C>A (GPSM2)	NP_037428.3:n.-493C>A
XM_005270787.2:c.-261C>A (GPSM2)	XP_005270844.1:n.-261C>A
XM_006710589.1:c.-246C>A (GPSM2)	XP_006710652.1:n.-246C>A
XM_011541301.1:c.-493C>A (GPSM2)	XP_011539603.1:n.-493C>A
XM_011541303.1:c.-493C>A (GPSM2)	XP_011539605.1:n.-493C>A
NM_001321038.1:c.-261C>A (GPSM2)	NP_001307967.1:n.-261C>A
NM_001321039.1:c.-493C>A (GPSM2)	NP_001307968.1:n.-493C>A
XM_006710589.3:c.-246C>A (GPSM2)	XP_006710652.1:n.-246C>A
XM_011541301.2:c.-493C>A (GPSM2)	XP_011539603.1:n.-493C>A
XM_011541302.3:c.-737C>A (GPSM2)	XP_011539604.1:n.-737C>A
XM_011541303.3:c.-493C>A (GPSM2)	XP_011539605.1:n.-493C>A
XM_017001097.2:c.-643C>A (GPSM2)	XP_016856586.1:n.-643C>A
XM_017001098.2:c.-411C>A (GPSM2)	XP_016856587.1:n.-411C>A