Canonical Allele Identifier: CA2655325661

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895403-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895403T>C , CM000684.2:g.19895403T>C	GRCh38
NC_000022.10:g.19882926T>C , CM000684.1:g.19882926T>C	GRCh37
NC_000022.9:g.18262926T>C	NCBI36
NG_011835.1:g.51434A>G , LRG_417:g.51434A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.949+4A>G MANE Select	ENSP00000383365.1:n.949+4A>G
ENST00000334363.14:c.949+4A>G	ENSP00000334451.9:n.949+4A>G
ENST00000400518.5:c.859+4A>G	ENSP00000383362.1:n.859+4A>G
ENST00000400519.6:c.946+4A>G	ENSP00000383363.1:n.946+4A>G
ENST00000400521.6:c.949+4A>G	ENSP00000383365.1:n.949+4A>G
ENST00000400525.6:c.880+4A>G	ENSP00000383369.3:n.880+4A>G
ENST00000474308.5:c.892+4A>G	ENSP00000485665.1:n.892+4A>G
ENST00000475995.3:c.446+4A>G
ENST00000491939.6:c.853+4A>G	ENSP00000485543.1:n.853+4A>G
ENST00000494454.5:n.1023+4A>G
ENST00000542719.6:c.661+4A>G	ENSP00000485128.2:n.661+4A>G
ENST00000634537.1:c.178+4A>G	ENSP00000489208.1:n.178+4A>G
ENST00000635155.1:n.535+4A>G
NM_001282512.1:c.949+4A>G	NP_001269441.1:n.949+4A>G
NM_006440.4:c.949+4A>G	NP_006431.2:n.949+4A>G
NM_001282512.2:c.949+4A>G	NP_001269441.1:n.949+4A>G
NM_001352300.1:c.946+4A>G	NP_001339229.1:n.946+4A>G
NM_001352301.1:c.859+4A>G	NP_001339230.1:n.859+4A>G
NM_001352302.1:c.661+4A>G	NP_001339231.1:n.661+4A>G
NM_001352303.1:c.853+4A>G	NP_001339232.1:n.853+4A>G
NR_147957.1:n.1081+4A>G
NM_006440.5:c.949+4A>G MANE Select	NP_006431.2:n.949+4A>G
NM_001282512.3:c.949+4A>G	NP_001269441.1:n.949+4A>G
NM_001352300.2:c.946+4A>G	NP_001339229.1:n.946+4A>G
NR_147957.2:n.907+4A>G
NM_001352301.2:c.859+4A>G	NP_001339230.1:n.859+4A>G
NM_001352302.2:c.661+4A>G	NP_001339231.1:n.661+4A>G
NM_001352303.2:c.853+4A>G	NP_001339232.1:n.853+4A>G