Canonical Allele Identifier: CA410686632

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883023T>C (hg19) ; chr22:g.19895500T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895500T>C , CM000684.2:g.19895500T>C	GRCh38
NC_000022.10:g.19883023T>C , CM000684.1:g.19883023T>C	GRCh37
NC_000022.9:g.18263023T>C	NCBI36
NG_011835.1:g.51337A>G , LRG_417:g.51337A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.856A>G MANE Select	ENSP00000383365.1:p.Arg286Gly
ENST00000334363.14:c.856A>G	ENSP00000334451.9:p.Arg286Gly
ENST00000400518.5:c.766A>G	ENSP00000383362.1:p.Arg256Gly
ENST00000400519.6:c.853A>G	ENSP00000383363.1:p.Arg285Gly
ENST00000400521.6:c.856A>G	ENSP00000383365.1:p.Arg286Gly
ENST00000400525.6:c.787A>G	ENSP00000383369.3:p.Arg263Gly
ENST00000474308.5:c.799A>G	ENSP00000485665.1:p.Arg267Gly
ENST00000475995.3:c.353A>G
ENST00000491939.6:c.760A>G	ENSP00000485543.1:p.Arg254Gly
ENST00000494454.5:n.930A>G
ENST00000542719.6:c.568A>G	ENSP00000485128.2:p.Arg190Gly
ENST00000634537.1:c.85A>G	ENSP00000489208.1:p.Arg29Gly
ENST00000635155.1:n.442A>G
NM_001282512.1:c.856A>G	NP_001269441.1:p.Arg286Gly
NM_006440.4:c.856A>G	NP_006431.2:p.Arg286Gly
NM_001282512.2:c.856A>G	NP_001269441.1:p.Arg286Gly
NM_001352300.1:c.853A>G	NP_001339229.1:p.Arg285Gly
NM_001352301.1:c.766A>G	NP_001339230.1:p.Arg256Gly
NM_001352302.1:c.568A>G	NP_001339231.1:p.Arg190Gly
NM_001352303.1:c.760A>G	NP_001339232.1:p.Arg254Gly
NR_147957.1:n.988A>G
NM_006440.5:c.856A>G MANE Select	NP_006431.2:p.Arg286Gly
NM_001282512.3:c.856A>G	NP_001269441.1:p.Arg286Gly
NM_001352300.2:c.853A>G	NP_001339229.1:p.Arg285Gly
NR_147957.2:n.814A>G
NM_001352301.2:c.766A>G	NP_001339230.1:p.Arg256Gly
NM_001352302.2:c.568A>G	NP_001339231.1:p.Arg190Gly
NM_001352303.2:c.760A>G	NP_001339232.1:p.Arg254Gly