Canonical Allele Identifier: CA751481164

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1302940502
• gnomAD v4: 22-19895372-C-T
• MyVariant Identifiers: chr22:g.19882895C>T (hg19) ; chr22:g.19895372C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895372C>T , CM000684.2:g.19895372C>T	GRCh38
NC_000022.10:g.19882895C>T , CM000684.1:g.19882895C>T	GRCh37
NC_000022.9:g.18262895C>T	NCBI36
NG_011835.1:g.51465G>A , LRG_417:g.51465G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.949+35G>A MANE Select	ENSP00000383365.1:n.949+35G>A
ENST00000334363.14:c.949+35G>A	ENSP00000334451.9:n.949+35G>A
ENST00000400518.5:c.859+35G>A	ENSP00000383362.1:n.859+35G>A
ENST00000400519.6:c.946+35G>A	ENSP00000383363.1:n.946+35G>A
ENST00000400521.6:c.949+35G>A	ENSP00000383365.1:n.949+35G>A
ENST00000400525.6:c.880+35G>A	ENSP00000383369.3:n.880+35G>A
ENST00000474308.5:c.892+35G>A	ENSP00000485665.1:n.892+35G>A
ENST00000475995.3:c.446+35G>A
ENST00000491939.6:c.853+35G>A	ENSP00000485543.1:n.853+35G>A
ENST00000494454.5:n.1023+35G>A
ENST00000542719.6:c.661+35G>A	ENSP00000485128.2:n.661+35G>A
ENST00000634537.1:c.178+35G>A	ENSP00000489208.1:n.178+35G>A
ENST00000635155.1:n.535+35G>A
NM_001282512.1:c.949+35G>A	NP_001269441.1:n.949+35G>A
NM_006440.4:c.949+35G>A	NP_006431.2:n.949+35G>A
NM_001282512.2:c.949+35G>A	NP_001269441.1:n.949+35G>A
NM_001352300.1:c.946+35G>A	NP_001339229.1:n.946+35G>A
NM_001352301.1:c.859+35G>A	NP_001339230.1:n.859+35G>A
NM_001352302.1:c.661+35G>A	NP_001339231.1:n.661+35G>A
NM_001352303.1:c.853+35G>A	NP_001339232.1:n.853+35G>A
NR_147957.1:n.1081+35G>A
NM_006440.5:c.949+35G>A MANE Select	NP_006431.2:n.949+35G>A
NM_001282512.3:c.949+35G>A	NP_001269441.1:n.949+35G>A
NM_001352300.2:c.946+35G>A	NP_001339229.1:n.946+35G>A
NR_147957.2:n.907+35G>A
NM_001352301.2:c.859+35G>A	NP_001339230.1:n.859+35G>A
NM_001352302.2:c.661+35G>A	NP_001339231.1:n.661+35G>A
NM_001352303.2:c.853+35G>A	NP_001339232.1:n.853+35G>A