Canonical Allele Identifier: CA4701142

Gene: GSR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30679524C>T , CM000670.2:g.30679524C>T	GRCh38
NC_000008.10:g.30537041C>T , CM000670.1:g.30537041C>T	GRCh37
NC_000008.9:g.30656583C>T	NCBI36
NG_027719.1:g.53446G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221130.11:c.1565G>A MANE Select	ENSP00000221130.5:p.Arg522His
ENST00000643525.1:n.1544G>A
ENST00000643653.1:c.1649G>A
ENST00000221130.9:c.1565G>A	ENSP00000221130.5:p.Arg522His
ENST00000537535.5:c.1319G>A	ENSP00000438845.1:p.Arg440His
ENST00000541648.5:c.1406G>A	ENSP00000444559.1:p.Arg469His
ENST00000546342.5:c.1478G>A	ENSP00000445516.1:p.Arg493His
NM_000637.3:c.1565G>A	NP_000628.2:p.Arg522His
NM_001195102.1:c.1478G>A	NP_001182031.1:p.Arg493His
NM_001195103.1:c.1406G>A	NP_001182032.1:p.Arg469His
NM_001195104.1:c.1319G>A	NP_001182033.1:p.Arg440His
NM_000637.4:c.1565G>A	NP_000628.2:p.Arg522His
NM_001195102.2:c.1478G>A	NP_001182031.1:p.Arg493His
NM_001195103.2:c.1406G>A	NP_001182032.1:p.Arg469His
NM_001195104.2:c.1319G>A	NP_001182033.1:p.Arg440His
NM_000637.5:c.1565G>A MANE Select	NP_000628.2:p.Arg522His
NM_001195102.3:c.1478G>A	NP_001182031.1:p.Arg493His
NM_001195103.3:c.1406G>A	NP_001182032.1:p.Arg469His
NM_001195104.3:c.1319G>A	NP_001182033.1:p.Arg440His