Canonical Allele Identifier: CA410686297

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882937C>G (hg19) ; chr22:g.19895414C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895414C>G , CM000684.2:g.19895414C>G	GRCh38
NC_000022.10:g.19882937C>G , CM000684.1:g.19882937C>G	GRCh37
NC_000022.9:g.18262937C>G	NCBI36
NG_011835.1:g.51423G>C , LRG_417:g.51423G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.942G>C MANE Select	ENSP00000383365.1:p.Trp314Cys
ENST00000334363.14:c.942G>C	ENSP00000334451.9:p.Trp314Cys
ENST00000400518.5:c.852G>C	ENSP00000383362.1:p.Trp284Cys
ENST00000400519.6:c.939G>C	ENSP00000383363.1:p.Trp313Cys
ENST00000400521.6:c.942G>C	ENSP00000383365.1:p.Trp314Cys
ENST00000400525.6:c.873G>C	ENSP00000383369.3:p.Trp291Cys
ENST00000474308.5:c.885G>C	ENSP00000485665.1:p.Trp295Cys
ENST00000475995.3:c.439G>C
ENST00000491939.6:c.846G>C	ENSP00000485543.1:p.Trp282Cys
ENST00000494454.5:n.1016G>C
ENST00000542719.6:c.654G>C	ENSP00000485128.2:p.Trp218Cys
ENST00000634537.1:c.171G>C	ENSP00000489208.1:p.Trp57Cys
ENST00000635155.1:n.528G>C
NM_001282512.1:c.942G>C	NP_001269441.1:p.Trp314Cys
NM_006440.4:c.942G>C	NP_006431.2:p.Trp314Cys
NM_001282512.2:c.942G>C	NP_001269441.1:p.Trp314Cys
NM_001352300.1:c.939G>C	NP_001339229.1:p.Trp313Cys
NM_001352301.1:c.852G>C	NP_001339230.1:p.Trp284Cys
NM_001352302.1:c.654G>C	NP_001339231.1:p.Trp218Cys
NM_001352303.1:c.846G>C	NP_001339232.1:p.Trp282Cys
NR_147957.1:n.1074G>C
NM_006440.5:c.942G>C MANE Select	NP_006431.2:p.Trp314Cys
NM_001282512.3:c.942G>C	NP_001269441.1:p.Trp314Cys
NM_001352300.2:c.939G>C	NP_001339229.1:p.Trp313Cys
NR_147957.2:n.900G>C
NM_001352301.2:c.852G>C	NP_001339230.1:p.Trp284Cys
NM_001352302.2:c.654G>C	NP_001339231.1:p.Trp218Cys
NM_001352303.2:c.846G>C	NP_001339232.1:p.Trp282Cys