Canonical Allele Identifier: CA410693759

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906425G>C (hg19) ; chr22:g.19918902G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918902G>C , CM000684.2:g.19918902G>C	GRCh38
NC_000022.10:g.19906425G>C , CM000684.1:g.19906425G>C	GRCh37
NC_000022.9:g.18286425G>C	NCBI36
NG_011835.1:g.27935C>G , LRG_417:g.27935C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.332C>G MANE Select	ENSP00000383365.1:p.Pro111Arg
ENST00000334363.14:c.332C>G	ENSP00000334451.9:p.Pro111Arg
ENST00000400518.5:c.242C>G	ENSP00000383362.1:p.Pro81Arg
ENST00000400519.6:c.329C>G	ENSP00000383363.1:p.Pro110Arg
ENST00000400521.6:c.332C>G	ENSP00000383365.1:p.Pro111Arg
ENST00000400525.6:c.263C>G	ENSP00000383369.3:p.Pro88Arg
ENST00000474308.5:c.275C>G	ENSP00000485665.1:p.Pro92Arg
ENST00000491939.6:c.236C>G	ENSP00000485543.1:p.Pro79Arg
ENST00000496729.2:n.337C>G
ENST00000542719.6:c.44C>G	ENSP00000485128.2:p.Pro15Arg
NM_001282512.1:c.332C>G	NP_001269441.1:p.Pro111Arg
NM_006440.4:c.332C>G	NP_006431.2:p.Pro111Arg
NM_001282512.2:c.332C>G	NP_001269441.1:p.Pro111Arg
NM_001352300.1:c.329C>G	NP_001339229.1:p.Pro110Arg
NM_001352301.1:c.242C>G	NP_001339230.1:p.Pro81Arg
NM_001352302.1:c.44C>G	NP_001339231.1:p.Pro15Arg
NM_001352303.1:c.236C>G	NP_001339232.1:p.Pro79Arg
NR_147957.1:n.464C>G
NM_006440.5:c.332C>G MANE Select	NP_006431.2:p.Pro111Arg
NM_001282512.3:c.332C>G	NP_001269441.1:p.Pro111Arg
NM_001352300.2:c.329C>G	NP_001339229.1:p.Pro110Arg
NR_147957.2:n.290C>G
NM_001352301.2:c.242C>G	NP_001339230.1:p.Pro81Arg
NM_001352302.2:c.44C>G	NP_001339231.1:p.Pro15Arg
NM_001352303.2:c.236C>G	NP_001339232.1:p.Pro79Arg