Canonical Allele Identifier: CA341456114

Gene: CLCC1 GPSM2 AKNAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.108896943T>C , CM000663.2:g.108896943T>C	GRCh38
NC_000001.10:g.109439565T>C , CM000663.1:g.109439565T>C	GRCh37
NC_000001.9:g.109241088T>C	NCBI36
NG_028108.1:g.24963T>C
NG_028108.2:g.26594T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_013296.5:c.136T>C (GPSM2) MANE Select	NP_037428.3:p.Phe46Leu
ENST00000264126.9:c.136T>C (GPSM2) MANE Select	ENSP00000264126.3:p.Phe46Leu
NM_001321038.1:c.136T>C (GPSM2)	NP_001307967.1:p.Phe46Leu
NM_001321038.2:c.136T>C (GPSM2)	NP_001307967.1:p.Phe46Leu
NM_001321039.1:c.136T>C (GPSM2)	NP_001307968.1:p.Phe46Leu
NM_001321039.2:c.136T>C (GPSM2)	NP_001307968.1:p.Phe46Leu
NM_001321039.3:c.136T>C (GPSM2)	NP_001307968.1:p.Phe46Leu
NM_013296.4:c.136T>C (GPSM2)	NP_037428.3:p.Phe46Leu
ENST00000264126.7:c.136T>C (GPSM2)	ENSP00000264126.3:p.Phe46Leu
ENST00000357393.5:c.115-47367A>G	ENSP00000349968.5:n.115-47367A>G
ENST00000357393.6:c.1-47367A>G (AKNAD1)	ENSP00000349968.6:n.1-47367A>G
ENST00000406462.6:c.136T>C (GPSM2)	ENSP00000385510.1:p.Phe46Leu
ENST00000435475.5:c.136T>C (GPSM2)	ENSP00000401948.1:p.Phe46Leu
ENST00000435987.5:c.136T>C (GPSM2)	ENSP00000408664.1:p.Phe46Leu
ENST00000441735.2:c.136T>C (GPSM2)	ENSP00000390629.2:p.Phe46Leu
ENST00000446797.1:c.136T>C (GPSM2)	ENSP00000392138.1:p.Phe46Leu
ENST00000446797.2:c.136T>C (GPSM2)	ENSP00000392138.2:p.Phe46Leu
ENST00000642355.1:c.136T>C (GPSM2)	ENSP00000496104.1:p.Phe46Leu
ENST00000643094.1:c.136T>C (GPSM2)	ENSP00000495317.1:p.Phe46Leu
ENST00000645164.2:c.136T>C (GPSM2)	ENSP00000496756.2:p.Phe46Leu
ENST00000674700.1:c.79T>C (GPSM2)	ENSP00000501743.1:p.Phe27Leu
ENST00000674731.1:c.79T>C (GPSM2)	ENSP00000502401.1:p.Phe27Leu
ENST00000674914.1:c.187T>C (GPSM2)	ENSP00000501579.1:p.Phe63Leu
ENST00000675086.1:c.136T>C (GPSM2)	ENSP00000502476.1:p.Phe46Leu
ENST00000675087.1:c.187T>C (GPSM2)	ENSP00000502020.1:p.Phe63Leu
ENST00000675617.1:n.698T>C (GPSM2)
ENST00000675776.1:n.631T>C (GPSM2)
ENST00000675829.1:n.653T>C (GPSM2)
ENST00000676184.1:c.136T>C (GPSM2)	ENSP00000502178.1:p.Phe46Leu
ENST00000676404.1:c.79T>C (GPSM2)	ENSP00000502346.1:p.Phe27Leu
ENST00000690509.1:c.*46-14695A>G (CLCC1)	ENSP00000510142.1:n.*46-14695A>G
XM_005270787.2:c.136T>C (GPSM2)	XP_005270844.1:p.Phe46Leu
XM_006710589.1:c.79T>C (GPSM2)	XP_006710652.1:p.Phe27Leu
XM_006710589.3:c.79T>C (GPSM2)	XP_006710652.1:p.Phe27Leu
XM_011541301.1:c.136T>C (GPSM2)	XP_011539603.1:p.Phe46Leu
XM_011541301.2:c.136T>C (GPSM2)	XP_011539603.1:p.Phe46Leu
XM_011541302.1:c.136T>C (GPSM2)	XP_011539604.1:p.Phe46Leu
XM_011541302.3:c.136T>C (GPSM2)	XP_011539604.1:p.Phe46Leu
XM_011541303.1:c.136T>C (GPSM2)	XP_011539605.1:p.Phe46Leu
XM_011541303.3:c.136T>C (GPSM2)	XP_011539605.1:p.Phe46Leu
XM_017001097.2:c.136T>C (GPSM2)	XP_016856586.1:p.Phe46Leu
XM_017001098.2:c.136T>C (GPSM2)	XP_016856587.1:p.Phe46Leu