Canonical Allele Identifier: CA513365619

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883102T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895579T>C , CM000684.2:g.19895579T>C	GRCh38
NC_000022.10:g.19883102T>C , CM000684.1:g.19883102T>C	GRCh37
NC_000022.9:g.18263102T>C	NCBI36
NG_011835.1:g.51258A>G , LRG_417:g.51258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.777A>G MANE Select	ENSP00000383365.1:p.Gln259=
ENST00000334363.14:c.777A>G	ENSP00000334451.9:p.Gln259=
ENST00000400518.5:c.687A>G	ENSP00000383362.1:p.Gln229=
ENST00000400519.6:c.774A>G	ENSP00000383363.1:p.Gln258=
ENST00000400521.6:c.777A>G	ENSP00000383365.1:p.Gln259=
ENST00000400525.6:c.708A>G	ENSP00000383369.3:p.Gln236=
ENST00000474308.5:c.720A>G	ENSP00000485665.1:p.Gln240=
ENST00000475995.3:c.274A>G
ENST00000491939.6:c.681A>G	ENSP00000485543.1:p.Gln227=
ENST00000494454.5:n.851A>G
ENST00000542719.6:c.489A>G	ENSP00000485128.2:p.Gln163=
ENST00000634537.1:c.6A>G	ENSP00000489208.1:p.Gln2=
ENST00000635155.1:n.363A>G
NM_001282512.1:c.777A>G	NP_001269441.1:p.Gln259=
NM_006440.4:c.777A>G	NP_006431.2:p.Gln259=
NM_001282512.2:c.777A>G	NP_001269441.1:p.Gln259=
NM_001352300.1:c.774A>G	NP_001339229.1:p.Gln258=
NM_001352301.1:c.687A>G	NP_001339230.1:p.Gln229=
NM_001352302.1:c.489A>G	NP_001339231.1:p.Gln163=
NM_001352303.1:c.681A>G	NP_001339232.1:p.Gln227=
NR_147957.1:n.909A>G
NM_006440.5:c.777A>G MANE Select	NP_006431.2:p.Gln259=
NM_001282512.3:c.777A>G	NP_001269441.1:p.Gln259=
NM_001352300.2:c.774A>G	NP_001339229.1:p.Gln258=
NR_147957.2:n.735A>G
NM_001352301.2:c.687A>G	NP_001339230.1:p.Gln229=
NM_001352302.2:c.489A>G	NP_001339231.1:p.Gln163=
NM_001352303.2:c.681A>G	NP_001339232.1:p.Gln227=