Canonical Allele Identifier: CA410686617

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895493-G-C
• MyVariant Identifiers: chr22:g.19883016G>C (hg19) ; chr22:g.19895493G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895493G>C , CM000684.2:g.19895493G>C	GRCh38
NC_000022.10:g.19883016G>C , CM000684.1:g.19883016G>C	GRCh37
NC_000022.9:g.18263016G>C	NCBI36
NG_011835.1:g.51344C>G , LRG_417:g.51344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.863C>G MANE Select	ENSP00000383365.1:p.Pro288Arg
ENST00000334363.14:c.863C>G	ENSP00000334451.9:p.Pro288Arg
ENST00000400518.5:c.773C>G	ENSP00000383362.1:p.Pro258Arg
ENST00000400519.6:c.860C>G	ENSP00000383363.1:p.Pro287Arg
ENST00000400521.6:c.863C>G	ENSP00000383365.1:p.Pro288Arg
ENST00000400525.6:c.794C>G	ENSP00000383369.3:p.Pro265Arg
ENST00000474308.5:c.806C>G	ENSP00000485665.1:p.Pro269Arg
ENST00000475995.3:c.360C>G
ENST00000491939.6:c.767C>G	ENSP00000485543.1:p.Pro256Arg
ENST00000494454.5:n.937C>G
ENST00000542719.6:c.575C>G	ENSP00000485128.2:p.Pro192Arg
ENST00000634537.1:c.92C>G	ENSP00000489208.1:p.Pro31Arg
ENST00000635155.1:n.449C>G
NM_001282512.1:c.863C>G	NP_001269441.1:p.Pro288Arg
NM_006440.4:c.863C>G	NP_006431.2:p.Pro288Arg
NM_001282512.2:c.863C>G	NP_001269441.1:p.Pro288Arg
NM_001352300.1:c.860C>G	NP_001339229.1:p.Pro287Arg
NM_001352301.1:c.773C>G	NP_001339230.1:p.Pro258Arg
NM_001352302.1:c.575C>G	NP_001339231.1:p.Pro192Arg
NM_001352303.1:c.767C>G	NP_001339232.1:p.Pro256Arg
NR_147957.1:n.995C>G
NM_006440.5:c.863C>G MANE Select	NP_006431.2:p.Pro288Arg
NM_001282512.3:c.863C>G	NP_001269441.1:p.Pro288Arg
NM_001352300.2:c.860C>G	NP_001339229.1:p.Pro287Arg
NR_147957.2:n.821C>G
NM_001352301.2:c.773C>G	NP_001339230.1:p.Pro258Arg
NM_001352302.2:c.575C>G	NP_001339231.1:p.Pro192Arg
NM_001352303.2:c.767C>G	NP_001339232.1:p.Pro256Arg