Canonical Allele Identifier: CA4701513

Gene: GSR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30708107G>A , CM000670.2:g.30708107G>A	GRCh38
NC_000008.10:g.30565624G>A , CM000670.1:g.30565624G>A	GRCh37
NC_000008.9:g.30685166G>A	NCBI36
NG_027719.1:g.24863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221130.11:c.457C>T MANE Select	ENSP00000221130.5:p.Arg153Cys
ENST00000643525.1:n.204C>T
ENST00000643653.1:c.323C>T
ENST00000221130.9:c.457C>T	ENSP00000221130.5:p.Arg153Cys
ENST00000521479.1:c.121C>T	ENSP00000430825.1:p.Arg41Cys
ENST00000523295.5:c.289C>T	ENSP00000431044.1:p.Arg97Cys
ENST00000537535.5:c.457C>T	ENSP00000438845.1:p.Arg153Cys
ENST00000541648.5:c.457C>T	ENSP00000444559.1:p.Arg153Cys
ENST00000546342.5:c.457C>T	ENSP00000445516.1:p.Arg153Cys
NM_000637.3:c.457C>T	NP_000628.2:p.Arg153Cys
NM_001195102.1:c.457C>T	NP_001182031.1:p.Arg153Cys
NM_001195103.1:c.457C>T	NP_001182032.1:p.Arg153Cys
NM_001195104.1:c.457C>T	NP_001182033.1:p.Arg153Cys
NM_000637.4:c.457C>T	NP_000628.2:p.Arg153Cys
NM_001195102.2:c.457C>T	NP_001182031.1:p.Arg153Cys
NM_001195103.2:c.457C>T	NP_001182032.1:p.Arg153Cys
NM_001195104.2:c.457C>T	NP_001182033.1:p.Arg153Cys
NM_000637.5:c.457C>T MANE Select	NP_000628.2:p.Arg153Cys
NM_001195102.3:c.457C>T	NP_001182031.1:p.Arg153Cys
NM_001195103.3:c.457C>T	NP_001182032.1:p.Arg153Cys
NM_001195104.3:c.457C>T	NP_001182033.1:p.Arg153Cys