Canonical Allele Identifier: CA410693834

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906446C>G (hg19) ; chr22:g.19918923C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918923C>G , CM000684.2:g.19918923C>G	GRCh38
NC_000022.10:g.19906446C>G , CM000684.1:g.19906446C>G	GRCh37
NC_000022.9:g.18286446C>G	NCBI36
NG_011835.1:g.27914G>C , LRG_417:g.27914G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.311G>C MANE Select	ENSP00000383365.1:p.Gly104Ala
ENST00000334363.14:c.311G>C	ENSP00000334451.9:p.Gly104Ala
ENST00000400518.5:c.221G>C	ENSP00000383362.1:p.Gly74Ala
ENST00000400519.6:c.308G>C	ENSP00000383363.1:p.Gly103Ala
ENST00000400521.6:c.311G>C	ENSP00000383365.1:p.Gly104Ala
ENST00000400525.6:c.242G>C	ENSP00000383369.3:p.Gly81Ala
ENST00000474308.5:c.254G>C	ENSP00000485665.1:p.Gly85Ala
ENST00000491939.6:c.215G>C	ENSP00000485543.1:p.Gly72Ala
ENST00000496729.2:n.316G>C
ENST00000542719.6:c.23G>C	ENSP00000485128.2:p.Gly8Ala
NM_001282512.1:c.311G>C	NP_001269441.1:p.Gly104Ala
NM_006440.4:c.311G>C	NP_006431.2:p.Gly104Ala
NM_001282512.2:c.311G>C	NP_001269441.1:p.Gly104Ala
NM_001352300.1:c.308G>C	NP_001339229.1:p.Gly103Ala
NM_001352301.1:c.221G>C	NP_001339230.1:p.Gly74Ala
NM_001352302.1:c.23G>C	NP_001339231.1:p.Gly8Ala
NM_001352303.1:c.215G>C	NP_001339232.1:p.Gly72Ala
NR_147957.1:n.443G>C
NM_006440.5:c.311G>C MANE Select	NP_006431.2:p.Gly104Ala
NM_001282512.3:c.311G>C	NP_001269441.1:p.Gly104Ala
NM_001352300.2:c.308G>C	NP_001339229.1:p.Gly103Ala
NR_147957.2:n.269G>C
NM_001352301.2:c.221G>C	NP_001339230.1:p.Gly74Ala
NM_001352302.2:c.23G>C	NP_001339231.1:p.Gly8Ala
NM_001352303.2:c.215G>C	NP_001339232.1:p.Gly72Ala