Canonical Allele Identifier: CA410686323

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882944A>G (hg19) ; chr22:g.19895421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895421A>G , CM000684.2:g.19895421A>G	GRCh38
NC_000022.10:g.19882944A>G , CM000684.1:g.19882944A>G	GRCh37
NC_000022.9:g.18262944A>G	NCBI36
NG_011835.1:g.51416T>C , LRG_417:g.51416T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.935T>C MANE Select	ENSP00000383365.1:p.Val312Ala
ENST00000334363.14:c.935T>C	ENSP00000334451.9:p.Val312Ala
ENST00000400518.5:c.845T>C	ENSP00000383362.1:p.Val282Ala
ENST00000400519.6:c.932T>C	ENSP00000383363.1:p.Val311Ala
ENST00000400521.6:c.935T>C	ENSP00000383365.1:p.Val312Ala
ENST00000400525.6:c.866T>C	ENSP00000383369.3:p.Val289Ala
ENST00000474308.5:c.878T>C	ENSP00000485665.1:p.Val293Ala
ENST00000475995.3:c.432T>C
ENST00000491939.6:c.839T>C	ENSP00000485543.1:p.Val280Ala
ENST00000494454.5:n.1009T>C
ENST00000542719.6:c.647T>C	ENSP00000485128.2:p.Val216Ala
ENST00000634537.1:c.164T>C	ENSP00000489208.1:p.Val55Ala
ENST00000635155.1:n.521T>C
NM_001282512.1:c.935T>C	NP_001269441.1:p.Val312Ala
NM_006440.4:c.935T>C	NP_006431.2:p.Val312Ala
NM_001282512.2:c.935T>C	NP_001269441.1:p.Val312Ala
NM_001352300.1:c.932T>C	NP_001339229.1:p.Val311Ala
NM_001352301.1:c.845T>C	NP_001339230.1:p.Val282Ala
NM_001352302.1:c.647T>C	NP_001339231.1:p.Val216Ala
NM_001352303.1:c.839T>C	NP_001339232.1:p.Val280Ala
NR_147957.1:n.1067T>C
NM_006440.5:c.935T>C MANE Select	NP_006431.2:p.Val312Ala
NM_001282512.3:c.935T>C	NP_001269441.1:p.Val312Ala
NM_001352300.2:c.932T>C	NP_001339229.1:p.Val311Ala
NR_147957.2:n.893T>C
NM_001352301.2:c.845T>C	NP_001339230.1:p.Val282Ala
NM_001352302.2:c.647T>C	NP_001339231.1:p.Val216Ala
NM_001352303.2:c.839T>C	NP_001339232.1:p.Val280Ala