Canonical Allele Identifier: CA513369037

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906394C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918871C>A , CM000684.2:g.19918871C>A	GRCh38
NC_000022.10:g.19906394C>A , CM000684.1:g.19906394C>A	GRCh37
NC_000022.9:g.18286394C>A	NCBI36
NG_011835.1:g.27966G>T , LRG_417:g.27966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.363G>T MANE Select	ENSP00000383365.1:p.Val121=
ENST00000334363.14:c.363G>T	ENSP00000334451.9:p.Val121=
ENST00000400518.5:c.273G>T	ENSP00000383362.1:p.Val91=
ENST00000400519.6:c.360G>T	ENSP00000383363.1:p.Val120=
ENST00000400521.6:c.363G>T	ENSP00000383365.1:p.Val121=
ENST00000400525.6:c.294G>T	ENSP00000383369.3:p.Val98=
ENST00000474308.5:c.306G>T	ENSP00000485665.1:p.Val102=
ENST00000491939.6:c.267G>T	ENSP00000485543.1:p.Val89=
ENST00000496729.2:n.368G>T
ENST00000542719.6:c.75G>T	ENSP00000485128.2:p.Val25=
NM_001282512.1:c.363G>T	NP_001269441.1:p.Val121=
NM_006440.4:c.363G>T	NP_006431.2:p.Val121=
NM_001282512.2:c.363G>T	NP_001269441.1:p.Val121=
NM_001352300.1:c.360G>T	NP_001339229.1:p.Val120=
NM_001352301.1:c.273G>T	NP_001339230.1:p.Val91=
NM_001352302.1:c.75G>T	NP_001339231.1:p.Val25=
NM_001352303.1:c.267G>T	NP_001339232.1:p.Val89=
NR_147957.1:n.495G>T
NM_006440.5:c.363G>T MANE Select	NP_006431.2:p.Val121=
NM_001282512.3:c.363G>T	NP_001269441.1:p.Val121=
NM_001352300.2:c.360G>T	NP_001339229.1:p.Val120=
NR_147957.2:n.321G>T
NM_001352301.2:c.273G>T	NP_001339230.1:p.Val91=
NM_001352302.2:c.75G>T	NP_001339231.1:p.Val25=
NM_001352303.2:c.267G>T	NP_001339232.1:p.Val89=