Canonical Allele Identifier: CA751493183

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1330782769
• MyVariant Identifiers: chr22:g.19906812G>A (hg19) ; chr22:g.19919289G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919289G>A , CM000684.2:g.19919289G>A	GRCh38
NC_000022.10:g.19906812G>A , CM000684.1:g.19906812G>A	GRCh37
NC_000022.9:g.18286812G>A	NCBI36
NG_011835.1:g.27548C>T , LRG_417:g.27548C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.229+254C>T MANE Select	ENSP00000383365.1:n.229+254C>T
ENST00000334363.14:c.229+254C>T	ENSP00000334451.9:n.229+254C>T
ENST00000400518.5:c.139+254C>T	ENSP00000383362.1:n.139+254C>T
ENST00000400519.6:c.226+254C>T	ENSP00000383363.1:n.226+254C>T
ENST00000400521.6:c.229+254C>T	ENSP00000383365.1:n.229+254C>T
ENST00000400525.6:c.160+254C>T	ENSP00000383369.3:n.160+254C>T
ENST00000474308.5:c.173-285C>T	ENSP00000485665.1:n.173-285C>T
ENST00000491939.6:c.133+254C>T	ENSP00000485543.1:n.133+254C>T
ENST00000496729.2:n.234+254C>T
ENST00000542719.6:c.-60+254C>T	ENSP00000485128.2:n.-60+254C>T
NM_001282512.1:c.229+254C>T	NP_001269441.1:n.229+254C>T
NM_006440.4:c.229+254C>T	NP_006431.2:n.229+254C>T
NM_001282512.2:c.229+254C>T	NP_001269441.1:n.229+254C>T
NM_001352300.1:c.226+254C>T	NP_001339229.1:n.226+254C>T
NM_001352301.1:c.139+254C>T	NP_001339230.1:n.139+254C>T
NM_001352302.1:c.-60+254C>T	NP_001339231.1:n.-60+254C>T
NM_001352303.1:c.133+254C>T	NP_001339232.1:n.133+254C>T
NR_147957.1:n.362-285C>T
NM_006440.5:c.229+254C>T MANE Select	NP_006431.2:n.229+254C>T
NM_001282512.3:c.229+254C>T	NP_001269441.1:n.229+254C>T
NM_001352300.2:c.226+254C>T	NP_001339229.1:n.226+254C>T
NR_147957.2:n.188-285C>T
NM_001352301.2:c.139+254C>T	NP_001339230.1:n.139+254C>T
NM_001352302.2:c.-60+254C>T	NP_001339231.1:n.-60+254C>T
NM_001352303.2:c.133+254C>T	NP_001339232.1:n.133+254C>T