Canonical Allele Identifier: CA410686443

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882966C>T (hg19) ; chr22:g.19895443C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895443C>T , CM000684.2:g.19895443C>T	GRCh38
NC_000022.10:g.19882966C>T , CM000684.1:g.19882966C>T	GRCh37
NC_000022.9:g.18262966C>T	NCBI36
NG_011835.1:g.51394G>A , LRG_417:g.51394G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.913G>A MANE Select	ENSP00000383365.1:p.Asp305Asn
ENST00000334363.14:c.913G>A	ENSP00000334451.9:p.Asp305Asn
ENST00000400518.5:c.823G>A	ENSP00000383362.1:p.Asp275Asn
ENST00000400519.6:c.910G>A	ENSP00000383363.1:p.Asp304Asn
ENST00000400521.6:c.913G>A	ENSP00000383365.1:p.Asp305Asn
ENST00000400525.6:c.844G>A	ENSP00000383369.3:p.Asp282Asn
ENST00000474308.5:c.856G>A	ENSP00000485665.1:p.Asp286Asn
ENST00000475995.3:c.410G>A
ENST00000491939.6:c.817G>A	ENSP00000485543.1:p.Asp273Asn
ENST00000494454.5:n.987G>A
ENST00000542719.6:c.625G>A	ENSP00000485128.2:p.Asp209Asn
ENST00000634537.1:c.142G>A	ENSP00000489208.1:p.Asp48Asn
ENST00000635155.1:n.499G>A
NM_001282512.1:c.913G>A	NP_001269441.1:p.Asp305Asn
NM_006440.4:c.913G>A	NP_006431.2:p.Asp305Asn
NM_001282512.2:c.913G>A	NP_001269441.1:p.Asp305Asn
NM_001352300.1:c.910G>A	NP_001339229.1:p.Asp304Asn
NM_001352301.1:c.823G>A	NP_001339230.1:p.Asp275Asn
NM_001352302.1:c.625G>A	NP_001339231.1:p.Asp209Asn
NM_001352303.1:c.817G>A	NP_001339232.1:p.Asp273Asn
NR_147957.1:n.1045G>A
NM_006440.5:c.913G>A MANE Select	NP_006431.2:p.Asp305Asn
NM_001282512.3:c.913G>A	NP_001269441.1:p.Asp305Asn
NM_001352300.2:c.910G>A	NP_001339229.1:p.Asp304Asn
NR_147957.2:n.871G>A
NM_001352301.2:c.823G>A	NP_001339230.1:p.Asp275Asn
NM_001352302.2:c.625G>A	NP_001339231.1:p.Asp209Asn
NM_001352303.2:c.817G>A	NP_001339232.1:p.Asp273Asn