Canonical Allele Identifier: CA4701286

Gene: GSR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30684172T>C , CM000670.2:g.30684172T>C	GRCh38
NC_000008.10:g.30541689T>C , CM000670.1:g.30541689T>C	GRCh37
NC_000008.9:g.30661231T>C	NCBI36
NG_027719.1:g.48798A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221130.11:c.1069A>G MANE Select	ENSP00000221130.5:p.Ile357Val
ENST00000643525.1:n.1048A>G
ENST00000643653.1:c.1153A>G
ENST00000221130.9:c.1069A>G	ENSP00000221130.5:p.Ile357Val
ENST00000523295.5:c.698A>G	ENSP00000431044.1:n.698A>G
ENST00000537535.5:c.823A>G	ENSP00000438845.1:p.Ile275Val
ENST00000541648.5:c.910A>G	ENSP00000444559.1:p.Ile304Val
ENST00000546342.5:c.982A>G	ENSP00000445516.1:p.Ile328Val
NM_000637.3:c.1069A>G	NP_000628.2:p.Ile357Val
NM_001195102.1:c.982A>G	NP_001182031.1:p.Ile328Val
NM_001195103.1:c.910A>G	NP_001182032.1:p.Ile304Val
NM_001195104.1:c.823A>G	NP_001182033.1:p.Ile275Val
NM_000637.4:c.1069A>G	NP_000628.2:p.Ile357Val
NM_001195102.2:c.982A>G	NP_001182031.1:p.Ile328Val
NM_001195103.2:c.910A>G	NP_001182032.1:p.Ile304Val
NM_001195104.2:c.823A>G	NP_001182033.1:p.Ile275Val
NM_000637.5:c.1069A>G MANE Select	NP_000628.2:p.Ile357Val
NM_001195102.3:c.982A>G	NP_001182031.1:p.Ile328Val
NM_001195103.3:c.910A>G	NP_001182032.1:p.Ile304Val
NM_001195104.3:c.823A>G	NP_001182033.1:p.Ile275Val