Canonical Allele Identifier: CA410693642

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906389T>G (hg19) ; chr22:g.19918866T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918866T>G , CM000684.2:g.19918866T>G	GRCh38
NC_000022.10:g.19906389T>G , CM000684.1:g.19906389T>G	GRCh37
NC_000022.9:g.18286389T>G	NCBI36
NG_011835.1:g.27971A>C , LRG_417:g.27971A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.368A>C MANE Select	ENSP00000383365.1:p.His123Pro
ENST00000334363.14:c.368A>C	ENSP00000334451.9:p.His123Pro
ENST00000400518.5:c.278A>C	ENSP00000383362.1:p.His93Pro
ENST00000400519.6:c.365A>C	ENSP00000383363.1:p.His122Pro
ENST00000400521.6:c.368A>C	ENSP00000383365.1:p.His123Pro
ENST00000400525.6:c.299A>C	ENSP00000383369.3:p.His100Pro
ENST00000474308.5:c.311A>C	ENSP00000485665.1:p.His104Pro
ENST00000491939.6:c.272A>C	ENSP00000485543.1:p.His91Pro
ENST00000496729.2:n.373A>C
ENST00000542719.6:c.80A>C	ENSP00000485128.2:p.His27Pro
NM_001282512.1:c.368A>C	NP_001269441.1:p.His123Pro
NM_006440.4:c.368A>C	NP_006431.2:p.His123Pro
NM_001282512.2:c.368A>C	NP_001269441.1:p.His123Pro
NM_001352300.1:c.365A>C	NP_001339229.1:p.His122Pro
NM_001352301.1:c.278A>C	NP_001339230.1:p.His93Pro
NM_001352302.1:c.80A>C	NP_001339231.1:p.His27Pro
NM_001352303.1:c.272A>C	NP_001339232.1:p.His91Pro
NR_147957.1:n.500A>C
NM_006440.5:c.368A>C MANE Select	NP_006431.2:p.His123Pro
NM_001282512.3:c.368A>C	NP_001269441.1:p.His123Pro
NM_001352300.2:c.365A>C	NP_001339229.1:p.His122Pro
NR_147957.2:n.326A>C
NM_001352301.2:c.278A>C	NP_001339230.1:p.His93Pro
NM_001352302.2:c.80A>C	NP_001339231.1:p.His27Pro
NM_001352303.2:c.272A>C	NP_001339232.1:p.His91Pro