Canonical Allele Identifier: CA2744980674

Gene: GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108877105dup , CM000663.2:g.108877105dup	GRCh38
NC_000001.10:g.109419727dup , CM000663.1:g.109419727dup	GRCh37
NC_000001.9:g.109221250dup	NCBI36
NG_028108.1:g.5125dup
NG_028108.2:g.6756dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264126.9:c.-372dup (GPSM2) MANE Select	ENSP00000264126.3:n.-372dup
ENST00000357393.6:c.1-27529dup (AKNAD1)	ENSP00000349968.6:n.1-27529dup
ENST00000441735.2:c.-290dup (GPSM2)	ENSP00000390629.2:n.-290dup
ENST00000642355.1:c.-372dup (GPSM2)	ENSP00000496104.1:n.-372dup
ENST00000643094.1:c.-418dup (GPSM2)	ENSP00000495317.1:n.-418dup
ENST00000645164.2:c.-186dup (GPSM2)	ENSP00000496756.2:n.-186dup
ENST00000674700.1:c.-125dup (GPSM2)	ENSP00000501743.1:n.-125dup
ENST00000674731.1:c.-125dup (GPSM2)	ENSP00000502401.1:n.-125dup
ENST00000674914.1:c.-183dup (GPSM2)	ENSP00000501579.1:n.-183dup
ENST00000675776.1:n.124dup (GPSM2)
ENST00000675829.1:n.146dup (GPSM2)
ENST00000676404.1:c.-125dup (GPSM2)	ENSP00000502346.1:n.-125dup
ENST00000264126.7:c.-372dup (GPSM2)	ENSP00000264126.3:n.-372dup
ENST00000357393.5:c.115-27529dup	ENSP00000349968.5:n.115-27529dup
ENST00000406462.6:c.-372dup (GPSM2)	ENSP00000385510.1:n.-372dup
ENST00000435987.5:c.-140dup (GPSM2)	ENSP00000408664.1:n.-140dup
NM_013296.4:c.-372dup (GPSM2)	NP_037428.3:n.-372dup
XM_005270787.2:c.-140dup (GPSM2)	XP_005270844.1:n.-140dup
XM_006710589.1:c.-125dup (GPSM2)	XP_006710652.1:n.-125dup
XM_011541301.1:c.-372dup (GPSM2)	XP_011539603.1:n.-372dup
XM_011541303.1:c.-372dup (GPSM2)	XP_011539605.1:n.-372dup
NM_001321038.1:c.-140dup (GPSM2)	NP_001307967.1:n.-140dup
NM_001321039.1:c.-372dup (GPSM2)	NP_001307968.1:n.-372dup
XM_006710589.3:c.-125dup (GPSM2)	XP_006710652.1:n.-125dup
XM_011541301.2:c.-372dup (GPSM2)	XP_011539603.1:n.-372dup
XM_011541302.3:c.-616dup (GPSM2)	XP_011539604.1:n.-616dup
XM_011541303.3:c.-372dup (GPSM2)	XP_011539605.1:n.-372dup
XM_017001097.2:c.-522dup (GPSM2)	XP_016856586.1:n.-522dup
XM_017001098.2:c.-290dup (GPSM2)	XP_016856587.1:n.-290dup
NM_013296.5:c.-372dup (GPSM2) MANE Select	NP_037428.3:n.-372dup
NM_001321038.2:c.-140dup (GPSM2)	NP_001307967.1:n.-140dup
NM_001321039.2:c.-372dup (GPSM2)	NP_001307968.1:n.-372dup
NM_001321039.3:c.-372dup (GPSM2)	NP_001307968.1:n.-372dup