Canonical Allele Identifier: CA322099126

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1053194982
• MyVariant Identifiers: chr22:g.19883285C>G (hg19) ; chr22:g.19895762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895762C>G , CM000684.2:g.19895762C>G	GRCh38
NC_000022.10:g.19883285C>G , CM000684.1:g.19883285C>G	GRCh37
NC_000022.9:g.18263285C>G	NCBI36
NG_011835.1:g.51075G>C , LRG_417:g.51075G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775-181G>C MANE Select	ENSP00000383365.1:n.775-181G>C
ENST00000334363.14:c.775-181G>C	ENSP00000334451.9:n.775-181G>C
ENST00000400518.5:c.685-181G>C	ENSP00000383362.1:n.685-181G>C
ENST00000400519.6:c.772-181G>C	ENSP00000383363.1:n.772-181G>C
ENST00000400521.6:c.775-181G>C	ENSP00000383365.1:n.775-181G>C
ENST00000400525.6:c.706-181G>C	ENSP00000383369.3:n.706-181G>C
ENST00000474308.5:c.718-181G>C	ENSP00000485665.1:n.718-181G>C
ENST00000475995.3:c.272-181G>C
ENST00000491939.6:c.679-181G>C	ENSP00000485543.1:n.679-181G>C
ENST00000494454.5:n.849-181G>C
ENST00000542719.6:c.487-181G>C	ENSP00000485128.2:n.487-181G>C
ENST00000634537.1:c.4-181G>C	ENSP00000489208.1:n.4-181G>C
ENST00000635155.1:n.361-181G>C
NM_001282512.1:c.775-181G>C	NP_001269441.1:n.775-181G>C
NM_006440.4:c.775-181G>C	NP_006431.2:n.775-181G>C
NM_001282512.2:c.775-181G>C	NP_001269441.1:n.775-181G>C
NM_001352300.1:c.772-181G>C	NP_001339229.1:n.772-181G>C
NM_001352301.1:c.685-181G>C	NP_001339230.1:n.685-181G>C
NM_001352302.1:c.487-181G>C	NP_001339231.1:n.487-181G>C
NM_001352303.1:c.679-181G>C	NP_001339232.1:n.679-181G>C
NR_147957.1:n.907-181G>C
NM_006440.5:c.775-181G>C MANE Select	NP_006431.2:n.775-181G>C
NM_001282512.3:c.775-181G>C	NP_001269441.1:n.775-181G>C
NM_001352300.2:c.772-181G>C	NP_001339229.1:n.772-181G>C
NR_147957.2:n.733-181G>C
NM_001352301.2:c.685-181G>C	NP_001339230.1:n.685-181G>C
NM_001352302.2:c.487-181G>C	NP_001339231.1:n.487-181G>C
NM_001352303.2:c.679-181G>C	NP_001339232.1:n.679-181G>C