Canonical Allele Identifier: CA410694075

Gene: TXNRD2

Linked Data

• dbSNP Id: rs2146047062
• MyVariant Identifiers: chr22:g.19906516C>G (hg19) ; chr22:g.19918993C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918993C>G , CM000684.2:g.19918993C>G	GRCh38
NC_000022.10:g.19906516C>G , CM000684.1:g.19906516C>G	GRCh37
NC_000022.9:g.18286516C>G	NCBI36
NG_011835.1:g.27844G>C , LRG_417:g.27844G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.241G>C MANE Select	ENSP00000383365.1:p.Gly81Arg
ENST00000334363.14:c.241G>C	ENSP00000334451.9:p.Gly81Arg
ENST00000400518.5:c.151G>C	ENSP00000383362.1:p.Gly51Arg
ENST00000400519.6:c.238G>C	ENSP00000383363.1:p.Gly80Arg
ENST00000400521.6:c.241G>C	ENSP00000383365.1:p.Gly81Arg
ENST00000400525.6:c.172G>C	ENSP00000383369.3:p.Gly58Arg
ENST00000474308.5:c.184G>C	ENSP00000485665.1:p.Gly62Arg
ENST00000491939.6:c.145G>C	ENSP00000485543.1:p.Gly49Arg
ENST00000496729.2:n.246G>C
ENST00000542719.6:c.-48G>C	ENSP00000485128.2:n.-48G>C
NM_001282512.1:c.241G>C	NP_001269441.1:p.Gly81Arg
NM_006440.4:c.241G>C	NP_006431.2:p.Gly81Arg
NM_001282512.2:c.241G>C	NP_001269441.1:p.Gly81Arg
NM_001352300.1:c.238G>C	NP_001339229.1:p.Gly80Arg
NM_001352301.1:c.151G>C	NP_001339230.1:p.Gly51Arg
NM_001352302.1:c.-48G>C	NP_001339231.1:n.-48G>C
NM_001352303.1:c.145G>C	NP_001339232.1:p.Gly49Arg
NR_147957.1:n.373G>C
NM_006440.5:c.241G>C MANE Select	NP_006431.2:p.Gly81Arg
NM_001282512.3:c.241G>C	NP_001269441.1:p.Gly81Arg
NM_001352300.2:c.238G>C	NP_001339229.1:p.Gly80Arg
NR_147957.2:n.199G>C
NM_001352301.2:c.151G>C	NP_001339230.1:p.Gly51Arg
NM_001352302.2:c.-48G>C	NP_001339231.1:n.-48G>C
NM_001352303.2:c.145G>C	NP_001339232.1:p.Gly49Arg