Canonical Allele Identifier: CA410694006

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906495T>C (hg19) ; chr22:g.19918972T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918972T>C , CM000684.2:g.19918972T>C	GRCh38
NC_000022.10:g.19906495T>C , CM000684.1:g.19906495T>C	GRCh37
NC_000022.9:g.18286495T>C	NCBI36
NG_011835.1:g.27865A>G , LRG_417:g.27865A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.262A>G MANE Select	ENSP00000383365.1:p.Asn88Asp
ENST00000334363.14:c.262A>G	ENSP00000334451.9:p.Asn88Asp
ENST00000400518.5:c.172A>G	ENSP00000383362.1:p.Asn58Asp
ENST00000400519.6:c.259A>G	ENSP00000383363.1:p.Asn87Asp
ENST00000400521.6:c.262A>G	ENSP00000383365.1:p.Asn88Asp
ENST00000400525.6:c.193A>G	ENSP00000383369.3:p.Asn65Asp
ENST00000474308.5:c.205A>G	ENSP00000485665.1:p.Asn69Asp
ENST00000491939.6:c.166A>G	ENSP00000485543.1:p.Asn56Asp
ENST00000496729.2:n.267A>G
ENST00000542719.6:c.-27A>G	ENSP00000485128.2:n.-27A>G
NM_001282512.1:c.262A>G	NP_001269441.1:p.Asn88Asp
NM_006440.4:c.262A>G	NP_006431.2:p.Asn88Asp
NM_001282512.2:c.262A>G	NP_001269441.1:p.Asn88Asp
NM_001352300.1:c.259A>G	NP_001339229.1:p.Asn87Asp
NM_001352301.1:c.172A>G	NP_001339230.1:p.Asn58Asp
NM_001352302.1:c.-27A>G	NP_001339231.1:n.-27A>G
NM_001352303.1:c.166A>G	NP_001339232.1:p.Asn56Asp
NR_147957.1:n.394A>G
NM_006440.5:c.262A>G MANE Select	NP_006431.2:p.Asn88Asp
NM_001282512.3:c.262A>G	NP_001269441.1:p.Asn88Asp
NM_001352300.2:c.259A>G	NP_001339229.1:p.Asn87Asp
NR_147957.2:n.220A>G
NM_001352301.2:c.172A>G	NP_001339230.1:p.Asn58Asp
NM_001352302.2:c.-27A>G	NP_001339231.1:n.-27A>G
NM_001352303.2:c.166A>G	NP_001339232.1:p.Asn56Asp