Canonical Allele Identifier: CA2646882521

Gene: GPSM2 AKNAD1

Linked Data

• gnomAD v4: 1-108877004-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108877004A>G , CM000663.2:g.108877004A>G	GRCh38
NC_000001.10:g.109419626A>G , CM000663.1:g.109419626A>G	GRCh37
NC_000001.9:g.109221149A>G	NCBI36
NG_028108.1:g.5024A>G
NG_028108.2:g.6655A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264126.9:c.-473A>G (GPSM2) MANE Select	ENSP00000264126.3:n.-473A>G
ENST00000357393.6:c.1-27428T>C (AKNAD1)	ENSP00000349968.6:n.1-27428T>C
ENST00000441735.2:c.-391A>G (GPSM2)	ENSP00000390629.2:n.-391A>G
ENST00000642355.1:c.-473A>G (GPSM2)	ENSP00000496104.1:n.-473A>G
ENST00000643094.1:c.-519A>G (GPSM2)	ENSP00000495317.1:n.-519A>G
ENST00000645164.2:c.-287A>G (GPSM2)	ENSP00000496756.2:n.-287A>G
ENST00000674700.1:c.-226A>G (GPSM2)	ENSP00000501743.1:n.-226A>G
ENST00000674731.1:c.-226A>G (GPSM2)	ENSP00000502401.1:n.-226A>G
ENST00000674914.1:c.-284A>G (GPSM2)	ENSP00000501579.1:n.-284A>G
ENST00000675776.1:n.23A>G (GPSM2)
ENST00000675829.1:n.45A>G (GPSM2)
ENST00000676404.1:c.-226A>G (GPSM2)	ENSP00000502346.1:n.-226A>G
ENST00000264126.7:c.-473A>G (GPSM2)	ENSP00000264126.3:n.-473A>G
ENST00000357393.5:c.115-27428T>C	ENSP00000349968.5:n.115-27428T>C
ENST00000406462.6:c.-473A>G (GPSM2)	ENSP00000385510.1:n.-473A>G
ENST00000435987.5:c.-241A>G (GPSM2)	ENSP00000408664.1:n.-241A>G
NM_013296.4:c.-473A>G (GPSM2)	NP_037428.3:n.-473A>G
XM_005270787.2:c.-241A>G (GPSM2)	XP_005270844.1:n.-241A>G
XM_006710589.1:c.-226A>G (GPSM2)	XP_006710652.1:n.-226A>G
XM_011541301.1:c.-473A>G (GPSM2)	XP_011539603.1:n.-473A>G
XM_011541303.1:c.-473A>G (GPSM2)	XP_011539605.1:n.-473A>G
NM_001321038.1:c.-241A>G (GPSM2)	NP_001307967.1:n.-241A>G
NM_001321039.1:c.-473A>G (GPSM2)	NP_001307968.1:n.-473A>G
XM_006710589.3:c.-226A>G (GPSM2)	XP_006710652.1:n.-226A>G
XM_011541301.2:c.-473A>G (GPSM2)	XP_011539603.1:n.-473A>G
XM_011541302.3:c.-717A>G (GPSM2)	XP_011539604.1:n.-717A>G
XM_011541303.3:c.-473A>G (GPSM2)	XP_011539605.1:n.-473A>G
XM_017001097.2:c.-623A>G (GPSM2)	XP_016856586.1:n.-623A>G
XM_017001098.2:c.-391A>G (GPSM2)	XP_016856587.1:n.-391A>G
NM_013296.5:c.-473A>G (GPSM2) MANE Select	NP_037428.3:n.-473A>G
NM_001321038.2:c.-241A>G (GPSM2)	NP_001307967.1:n.-241A>G
NM_001321039.2:c.-473A>G (GPSM2)	NP_001307968.1:n.-473A>G
NM_001321039.3:c.-473A>G (GPSM2)	NP_001307968.1:n.-473A>G