Canonical Allele Identifier: CA4701574

Gene: GSR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30712088C>T , CM000670.2:g.30712088C>T	GRCh38
NC_000008.10:g.30569605C>T , CM000670.1:g.30569605C>T	GRCh37
NC_000008.9:g.30689147C>T	NCBI36
NG_027719.1:g.20882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221130.11:c.307G>A MANE Select	ENSP00000221130.5:p.Val103Met
ENST00000643525.1:n.54G>A
ENST00000643653.1:c.173G>A
ENST00000221130.9:c.307G>A	ENSP00000221130.5:p.Val103Met
ENST00000521479.1:c.-30G>A	ENSP00000430825.1:n.-30G>A
ENST00000523295.5:c.139G>A	ENSP00000431044.1:p.Val47Met
ENST00000537535.5:c.307G>A	ENSP00000438845.1:p.Val103Met
ENST00000541648.5:c.307G>A	ENSP00000444559.1:p.Val103Met
ENST00000546342.5:c.307G>A	ENSP00000445516.1:p.Val103Met
NM_000637.3:c.307G>A	NP_000628.2:p.Val103Met
NM_001195102.1:c.307G>A	NP_001182031.1:p.Val103Met
NM_001195103.1:c.307G>A	NP_001182032.1:p.Val103Met
NM_001195104.1:c.307G>A	NP_001182033.1:p.Val103Met
NM_000637.4:c.307G>A	NP_000628.2:p.Val103Met
NM_001195102.2:c.307G>A	NP_001182031.1:p.Val103Met
NM_001195103.2:c.307G>A	NP_001182032.1:p.Val103Met
NM_001195104.2:c.307G>A	NP_001182033.1:p.Val103Met
NM_000637.5:c.307G>A MANE Select	NP_000628.2:p.Val103Met
NM_001195102.3:c.307G>A	NP_001182031.1:p.Val103Met
NM_001195103.3:c.307G>A	NP_001182032.1:p.Val103Met
NM_001195104.3:c.307G>A	NP_001182033.1:p.Val103Met