Canonical Allele Identifier: CA410686566

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882992C>G (hg19) ; chr22:g.19895469C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895469C>G , CM000684.2:g.19895469C>G	GRCh38
NC_000022.10:g.19882992C>G , CM000684.1:g.19882992C>G	GRCh37
NC_000022.9:g.18262992C>G	NCBI36
NG_011835.1:g.51368G>C , LRG_417:g.51368G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.887G>C MANE Select	ENSP00000383365.1:p.Trp296Ser
ENST00000334363.14:c.887G>C	ENSP00000334451.9:p.Trp296Ser
ENST00000400518.5:c.797G>C	ENSP00000383362.1:p.Trp266Ser
ENST00000400519.6:c.884G>C	ENSP00000383363.1:p.Trp295Ser
ENST00000400521.6:c.887G>C	ENSP00000383365.1:p.Trp296Ser
ENST00000400525.6:c.818G>C	ENSP00000383369.3:p.Trp273Ser
ENST00000474308.5:c.830G>C	ENSP00000485665.1:p.Trp277Ser
ENST00000475995.3:c.384G>C
ENST00000491939.6:c.791G>C	ENSP00000485543.1:p.Trp264Ser
ENST00000494454.5:n.961G>C
ENST00000542719.6:c.599G>C	ENSP00000485128.2:p.Trp200Ser
ENST00000634537.1:c.116G>C	ENSP00000489208.1:p.Trp39Ser
ENST00000635155.1:n.473G>C
NM_001282512.1:c.887G>C	NP_001269441.1:p.Trp296Ser
NM_006440.4:c.887G>C	NP_006431.2:p.Trp296Ser
NM_001282512.2:c.887G>C	NP_001269441.1:p.Trp296Ser
NM_001352300.1:c.884G>C	NP_001339229.1:p.Trp295Ser
NM_001352301.1:c.797G>C	NP_001339230.1:p.Trp266Ser
NM_001352302.1:c.599G>C	NP_001339231.1:p.Trp200Ser
NM_001352303.1:c.791G>C	NP_001339232.1:p.Trp264Ser
NR_147957.1:n.1019G>C
NM_006440.5:c.887G>C MANE Select	NP_006431.2:p.Trp296Ser
NM_001282512.3:c.887G>C	NP_001269441.1:p.Trp296Ser
NM_001352300.2:c.884G>C	NP_001339229.1:p.Trp295Ser
NR_147957.2:n.845G>C
NM_001352301.2:c.797G>C	NP_001339230.1:p.Trp266Ser
NM_001352302.2:c.599G>C	NP_001339231.1:p.Trp200Ser
NM_001352303.2:c.791G>C	NP_001339232.1:p.Trp264Ser