Canonical Allele Identifier: CA410693669

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906400C>G (hg19) ; chr22:g.19918877C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918877C>G , CM000684.2:g.19918877C>G	GRCh38
NC_000022.10:g.19906400C>G , CM000684.1:g.19906400C>G	GRCh37
NC_000022.9:g.18286400C>G	NCBI36
NG_011835.1:g.27960G>C , LRG_417:g.27960G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.357G>C MANE Select	ENSP00000383365.1:p.Gln119His
ENST00000334363.14:c.357G>C	ENSP00000334451.9:p.Gln119His
ENST00000400518.5:c.267G>C	ENSP00000383362.1:p.Gln89His
ENST00000400519.6:c.354G>C	ENSP00000383363.1:p.Gln118His
ENST00000400521.6:c.357G>C	ENSP00000383365.1:p.Gln119His
ENST00000400525.6:c.288G>C	ENSP00000383369.3:p.Gln96His
ENST00000474308.5:c.300G>C	ENSP00000485665.1:p.Gln100His
ENST00000491939.6:c.261G>C	ENSP00000485543.1:p.Gln87His
ENST00000496729.2:n.362G>C
ENST00000542719.6:c.69G>C	ENSP00000485128.2:p.Gln23His
NM_001282512.1:c.357G>C	NP_001269441.1:p.Gln119His
NM_006440.4:c.357G>C	NP_006431.2:p.Gln119His
NM_001282512.2:c.357G>C	NP_001269441.1:p.Gln119His
NM_001352300.1:c.354G>C	NP_001339229.1:p.Gln118His
NM_001352301.1:c.267G>C	NP_001339230.1:p.Gln89His
NM_001352302.1:c.69G>C	NP_001339231.1:p.Gln23His
NM_001352303.1:c.261G>C	NP_001339232.1:p.Gln87His
NR_147957.1:n.489G>C
NM_006440.5:c.357G>C MANE Select	NP_006431.2:p.Gln119His
NM_001282512.3:c.357G>C	NP_001269441.1:p.Gln119His
NM_001352300.2:c.354G>C	NP_001339229.1:p.Gln118His
NR_147957.2:n.315G>C
NM_001352301.2:c.267G>C	NP_001339230.1:p.Gln89His
NM_001352302.2:c.69G>C	NP_001339231.1:p.Gln23His
NM_001352303.2:c.261G>C	NP_001339232.1:p.Gln87His