Canonical Allele Identifier: CA1187870765

Gene: GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108877061G= , CM000663.2:g.108877061G=	GRCh38
NC_000001.10:g.109419683G= , CM000663.1:g.109419683G=	GRCh37
NC_000001.9:g.109221206G=	NCBI36
NG_028108.1:g.5081G=
NG_028108.2:g.6712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264126.9:c.-416G= (GPSM2) MANE Select	ENSP00000264126.3:n.-416G=
ENST00000357393.6:c.1-27485C= (AKNAD1)	ENSP00000349968.6:n.1-27485C=
ENST00000441735.2:c.-334G= (GPSM2)	ENSP00000390629.2:n.-334G=
ENST00000642355.1:c.-416G= (GPSM2)	ENSP00000496104.1:n.-416G=
ENST00000643094.1:c.-462G= (GPSM2)	ENSP00000495317.1:n.-462G=
ENST00000645164.2:c.-230G= (GPSM2)	ENSP00000496756.2:n.-230G=
ENST00000674700.1:c.-169G= (GPSM2)	ENSP00000501743.1:n.-169G=
ENST00000674731.1:c.-169G= (GPSM2)	ENSP00000502401.1:n.-169G=
ENST00000674914.1:c.-227G= (GPSM2)	ENSP00000501579.1:n.-227G=
ENST00000675776.1:n.80G= (GPSM2)
ENST00000675829.1:n.102G= (GPSM2)
ENST00000676404.1:c.-169G= (GPSM2)	ENSP00000502346.1:n.-169G=
ENST00000264126.7:c.-416G= (GPSM2)	ENSP00000264126.3:n.-416G=
ENST00000357393.5:c.115-27485C=	ENSP00000349968.5:n.115-27485C=
ENST00000406462.6:c.-416G= (GPSM2)	ENSP00000385510.1:n.-416G=
ENST00000435987.5:c.-184G= (GPSM2)	ENSP00000408664.1:n.-184G=
NM_013296.4:c.-416G= (GPSM2)	NP_037428.3:n.-416G=
XM_005270787.2:c.-184G= (GPSM2)	XP_005270844.1:n.-184G=
XM_006710589.1:c.-169G= (GPSM2)	XP_006710652.1:n.-169G=
XM_011541301.1:c.-416G= (GPSM2)	XP_011539603.1:n.-416G=
XM_011541303.1:c.-416G= (GPSM2)	XP_011539605.1:n.-416G=
NM_001321038.1:c.-184G= (GPSM2)	NP_001307967.1:n.-184G=
NM_001321039.1:c.-416G= (GPSM2)	NP_001307968.1:n.-416G=
XM_006710589.3:c.-169G= (GPSM2)	XP_006710652.1:n.-169G=
XM_011541301.2:c.-416G= (GPSM2)	XP_011539603.1:n.-416G=
XM_011541302.3:c.-660G= (GPSM2)	XP_011539604.1:n.-660G=
XM_011541303.3:c.-416G= (GPSM2)	XP_011539605.1:n.-416G=
XM_017001097.2:c.-566G= (GPSM2)	XP_016856586.1:n.-566G=
XM_017001098.2:c.-334G= (GPSM2)	XP_016856587.1:n.-334G=
NM_013296.5:c.-416G= (GPSM2) MANE Select	NP_037428.3:n.-416G=
NM_001321038.2:c.-184G= (GPSM2)	NP_001307967.1:n.-184G=
NM_001321039.2:c.-416G= (GPSM2)	NP_001307968.1:n.-416G=
NM_001321039.3:c.-416G= (GPSM2)	NP_001307968.1:n.-416G=