Canonical Allele Identifier: CA2646882524

Gene: GPSM2 AKNAD1

Linked Data

• gnomAD v4: 1-108877010-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108877010G>T , CM000663.2:g.108877010G>T	GRCh38
NC_000001.10:g.109419632G>T , CM000663.1:g.109419632G>T	GRCh37
NC_000001.9:g.109221155G>T	NCBI36
NG_028108.1:g.5030G>T
NG_028108.2:g.6661G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264126.9:c.-467G>T (GPSM2) MANE Select	ENSP00000264126.3:n.-467G>T
ENST00000357393.6:c.1-27434C>A (AKNAD1)	ENSP00000349968.6:n.1-27434C>A
ENST00000441735.2:c.-385G>T (GPSM2)	ENSP00000390629.2:n.-385G>T
ENST00000642355.1:c.-467G>T (GPSM2)	ENSP00000496104.1:n.-467G>T
ENST00000643094.1:c.-513G>T (GPSM2)	ENSP00000495317.1:n.-513G>T
ENST00000645164.2:c.-281G>T (GPSM2)	ENSP00000496756.2:n.-281G>T
ENST00000674700.1:c.-220G>T (GPSM2)	ENSP00000501743.1:n.-220G>T
ENST00000674731.1:c.-220G>T (GPSM2)	ENSP00000502401.1:n.-220G>T
ENST00000674914.1:c.-278G>T (GPSM2)	ENSP00000501579.1:n.-278G>T
ENST00000675776.1:n.29G>T (GPSM2)
ENST00000675829.1:n.51G>T (GPSM2)
ENST00000676404.1:c.-220G>T (GPSM2)	ENSP00000502346.1:n.-220G>T
ENST00000264126.7:c.-467G>T (GPSM2)	ENSP00000264126.3:n.-467G>T
ENST00000357393.5:c.115-27434C>A	ENSP00000349968.5:n.115-27434C>A
ENST00000406462.6:c.-467G>T (GPSM2)	ENSP00000385510.1:n.-467G>T
ENST00000435987.5:c.-235G>T (GPSM2)	ENSP00000408664.1:n.-235G>T
NM_013296.4:c.-467G>T (GPSM2)	NP_037428.3:n.-467G>T
XM_005270787.2:c.-235G>T (GPSM2)	XP_005270844.1:n.-235G>T
XM_006710589.1:c.-220G>T (GPSM2)	XP_006710652.1:n.-220G>T
XM_011541301.1:c.-467G>T (GPSM2)	XP_011539603.1:n.-467G>T
XM_011541303.1:c.-467G>T (GPSM2)	XP_011539605.1:n.-467G>T
NM_001321038.1:c.-235G>T (GPSM2)	NP_001307967.1:n.-235G>T
NM_001321039.1:c.-467G>T (GPSM2)	NP_001307968.1:n.-467G>T
XM_006710589.3:c.-220G>T (GPSM2)	XP_006710652.1:n.-220G>T
XM_011541301.2:c.-467G>T (GPSM2)	XP_011539603.1:n.-467G>T
XM_011541302.3:c.-711G>T (GPSM2)	XP_011539604.1:n.-711G>T
XM_011541303.3:c.-467G>T (GPSM2)	XP_011539605.1:n.-467G>T
XM_017001097.2:c.-617G>T (GPSM2)	XP_016856586.1:n.-617G>T
XM_017001098.2:c.-385G>T (GPSM2)	XP_016856587.1:n.-385G>T
NM_013296.5:c.-467G>T (GPSM2) MANE Select	NP_037428.3:n.-467G>T
NM_001321038.2:c.-235G>T (GPSM2)	NP_001307967.1:n.-235G>T
NM_001321039.2:c.-467G>T (GPSM2)	NP_001307968.1:n.-467G>T
NM_001321039.3:c.-467G>T (GPSM2)	NP_001307968.1:n.-467G>T