Canonical Allele Identifier: CA10104079

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19911383C>G , CM000684.2:g.19911383C>G	GRCh38
NC_000022.10:g.19898906C>G , CM000684.1:g.19898906C>G	GRCh37
NC_000022.9:g.18278906C>G	NCBI36
NG_011835.1:g.35454G>C , LRG_417:g.35454G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.656G>C MANE Select	NP_006431.2:p.Gly219Ala
ENST00000400521.7:c.656G>C MANE Select	ENSP00000383365.1:p.Gly219Ala
NM_001282512.1:c.656G>C	NP_001269441.1:p.Gly219Ala
NM_001282512.2:c.656G>C	NP_001269441.1:p.Gly219Ala
NM_001282512.3:c.656G>C	NP_001269441.1:p.Gly219Ala
NM_001352300.1:c.653G>C	NP_001339229.1:p.Gly218Ala
NM_001352300.2:c.653G>C	NP_001339229.1:p.Gly218Ala
NM_001352301.1:c.566G>C	NP_001339230.1:p.Gly189Ala
NM_001352301.2:c.566G>C	NP_001339230.1:p.Gly189Ala
NM_001352302.1:c.368G>C	NP_001339231.1:p.Gly123Ala
NM_001352302.2:c.368G>C	NP_001339231.1:p.Gly123Ala
NM_001352303.1:c.560G>C	NP_001339232.1:p.Gly187Ala
NM_001352303.2:c.560G>C	NP_001339232.1:p.Gly187Ala
NM_006440.4:c.656G>C	NP_006431.2:p.Gly219Ala
NR_147957.1:n.788G>C
NR_147957.2:n.614G>C
ENST00000334363.14:c.656G>C	ENSP00000334451.9:p.Gly219Ala
ENST00000400518.5:c.566G>C	ENSP00000383362.1:p.Gly189Ala
ENST00000400519.6:c.653G>C	ENSP00000383363.1:p.Gly218Ala
ENST00000400521.6:c.656G>C	ENSP00000383365.1:p.Gly219Ala
ENST00000400525.6:c.587G>C	ENSP00000383369.3:p.Gly196Ala
ENST00000471835.1:n.201G>C
ENST00000474308.5:c.599G>C	ENSP00000485665.1:p.Gly200Ala
ENST00000475995.3:c.153G>C
ENST00000484672.5:n.286G>C
ENST00000491939.6:c.560G>C	ENSP00000485543.1:p.Gly187Ala
ENST00000494454.5:n.730G>C
ENST00000542719.6:c.368G>C	ENSP00000485128.2:p.Gly123Ala
ENST00000635155.1:n.242G>C