Canonical Allele Identifier: CA410686657

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883040G>T (hg19) ; chr22:g.19895517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895517G>T , CM000684.2:g.19895517G>T	GRCh38
NC_000022.10:g.19883040G>T , CM000684.1:g.19883040G>T	GRCh37
NC_000022.9:g.18263040G>T	NCBI36
NG_011835.1:g.51320C>A , LRG_417:g.51320C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.839C>A MANE Select	ENSP00000383365.1:p.Ala280Asp
ENST00000334363.14:c.839C>A	ENSP00000334451.9:p.Ala280Asp
ENST00000400518.5:c.749C>A	ENSP00000383362.1:p.Ala250Asp
ENST00000400519.6:c.836C>A	ENSP00000383363.1:p.Ala279Asp
ENST00000400521.6:c.839C>A	ENSP00000383365.1:p.Ala280Asp
ENST00000400525.6:c.770C>A	ENSP00000383369.3:p.Ala257Asp
ENST00000474308.5:c.782C>A	ENSP00000485665.1:p.Ala261Asp
ENST00000475995.3:c.336C>A
ENST00000491939.6:c.743C>A	ENSP00000485543.1:p.Ala248Asp
ENST00000494454.5:n.913C>A
ENST00000542719.6:c.551C>A	ENSP00000485128.2:p.Ala184Asp
ENST00000634537.1:c.68C>A	ENSP00000489208.1:p.Ala23Asp
ENST00000635155.1:n.425C>A
NM_001282512.1:c.839C>A	NP_001269441.1:p.Ala280Asp
NM_006440.4:c.839C>A	NP_006431.2:p.Ala280Asp
NM_001282512.2:c.839C>A	NP_001269441.1:p.Ala280Asp
NM_001352300.1:c.836C>A	NP_001339229.1:p.Ala279Asp
NM_001352301.1:c.749C>A	NP_001339230.1:p.Ala250Asp
NM_001352302.1:c.551C>A	NP_001339231.1:p.Ala184Asp
NM_001352303.1:c.743C>A	NP_001339232.1:p.Ala248Asp
NR_147957.1:n.971C>A
NM_006440.5:c.839C>A MANE Select	NP_006431.2:p.Ala280Asp
NM_001282512.3:c.839C>A	NP_001269441.1:p.Ala280Asp
NM_001352300.2:c.836C>A	NP_001339229.1:p.Ala279Asp
NR_147957.2:n.797C>A
NM_001352301.2:c.749C>A	NP_001339230.1:p.Ala250Asp
NM_001352302.2:c.551C>A	NP_001339231.1:p.Ala184Asp
NM_001352303.2:c.743C>A	NP_001339232.1:p.Ala248Asp