Canonical Allele Identifier: CA2838553056

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19899143dup , CM000684.2:g.19899143dup	GRCh38
NC_000022.10:g.19886666dup , CM000684.1:g.19886666dup	GRCh37
NC_000022.9:g.18266666dup	NCBI36
NG_011835.1:g.47697dup , LRG_417:g.47697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.663-72dup MANE Select	ENSP00000383365.1:n.663-72dup
ENST00000334363.14:c.663-72dup	ENSP00000334451.9:n.663-72dup
ENST00000400518.5:c.573-72dup	ENSP00000383362.1:n.573-72dup
ENST00000400519.6:c.660-72dup	ENSP00000383363.1:n.660-72dup
ENST00000400521.6:c.663-72dup	ENSP00000383365.1:n.663-72dup
ENST00000400525.6:c.594-72dup	ENSP00000383369.3:n.594-72dup
ENST00000474308.5:c.606-72dup	ENSP00000485665.1:n.606-72dup
ENST00000475995.3:c.160-72dup
ENST00000491939.6:c.567-72dup	ENSP00000485543.1:n.567-72dup
ENST00000494454.5:n.737-72dup
ENST00000542719.6:c.375-72dup	ENSP00000485128.2:n.375-72dup
ENST00000635155.1:n.249-72dup
NM_001282512.1:c.663-72dup	NP_001269441.1:n.663-72dup
NM_006440.4:c.663-72dup	NP_006431.2:n.663-72dup
NM_001282512.2:c.663-72dup	NP_001269441.1:n.663-72dup
NM_001352300.1:c.660-72dup	NP_001339229.1:n.660-72dup
NM_001352301.1:c.573-72dup	NP_001339230.1:n.573-72dup
NM_001352302.1:c.375-72dup	NP_001339231.1:n.375-72dup
NM_001352303.1:c.567-72dup	NP_001339232.1:n.567-72dup
NR_147957.1:n.795-72dup
NM_006440.5:c.663-72dup MANE Select	NP_006431.2:n.663-72dup
NM_001282512.3:c.663-72dup	NP_001269441.1:n.663-72dup
NM_001352300.2:c.660-72dup	NP_001339229.1:n.660-72dup
NR_147957.2:n.621-72dup
NM_001352301.2:c.573-72dup	NP_001339230.1:n.573-72dup
NM_001352302.2:c.375-72dup	NP_001339231.1:n.375-72dup
NM_001352303.2:c.567-72dup	NP_001339232.1:n.567-72dup