Canonical Allele Identifier: CA513365203

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883015A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895492A>G , CM000684.2:g.19895492A>G	GRCh38
NC_000022.10:g.19883015A>G , CM000684.1:g.19883015A>G	GRCh37
NC_000022.9:g.18263015A>G	NCBI36
NG_011835.1:g.51345T>C , LRG_417:g.51345T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.864T>C MANE Select	ENSP00000383365.1:p.Pro288=
ENST00000334363.14:c.864T>C	ENSP00000334451.9:p.Pro288=
ENST00000400518.5:c.774T>C	ENSP00000383362.1:p.Pro258=
ENST00000400519.6:c.861T>C	ENSP00000383363.1:p.Pro287=
ENST00000400521.6:c.864T>C	ENSP00000383365.1:p.Pro288=
ENST00000400525.6:c.795T>C	ENSP00000383369.3:p.Pro265=
ENST00000474308.5:c.807T>C	ENSP00000485665.1:p.Pro269=
ENST00000475995.3:c.361T>C
ENST00000491939.6:c.768T>C	ENSP00000485543.1:p.Pro256=
ENST00000494454.5:n.938T>C
ENST00000542719.6:c.576T>C	ENSP00000485128.2:p.Pro192=
ENST00000634537.1:c.93T>C	ENSP00000489208.1:p.Pro31=
ENST00000635155.1:n.450T>C
NM_001282512.1:c.864T>C	NP_001269441.1:p.Pro288=
NM_006440.4:c.864T>C	NP_006431.2:p.Pro288=
NM_001282512.2:c.864T>C	NP_001269441.1:p.Pro288=
NM_001352300.1:c.861T>C	NP_001339229.1:p.Pro287=
NM_001352301.1:c.774T>C	NP_001339230.1:p.Pro258=
NM_001352302.1:c.576T>C	NP_001339231.1:p.Pro192=
NM_001352303.1:c.768T>C	NP_001339232.1:p.Pro256=
NR_147957.1:n.996T>C
NM_006440.5:c.864T>C MANE Select	NP_006431.2:p.Pro288=
NM_001282512.3:c.864T>C	NP_001269441.1:p.Pro288=
NM_001352300.2:c.861T>C	NP_001339229.1:p.Pro287=
NR_147957.2:n.822T>C
NM_001352301.2:c.774T>C	NP_001339230.1:p.Pro258=
NM_001352302.2:c.576T>C	NP_001339231.1:p.Pro192=
NM_001352303.2:c.768T>C	NP_001339232.1:p.Pro256=