Canonical Allele Identifier: CA410681904

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868156C>T (hg19) ; chr22:g.19880633C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880633C>T , CM000684.2:g.19880633C>T	GRCh38
NC_000022.10:g.19868156C>T , CM000684.1:g.19868156C>T	GRCh37
NC_000022.9:g.18248156C>T	NCBI36
NG_011835.1:g.66204G>A , LRG_417:g.66204G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1171G>A MANE Select	ENSP00000383365.1:p.Asp391Asn
ENST00000400518.5:c.1081G>A	ENSP00000383362.1:p.Asp361Asn
ENST00000400519.6:c.1168G>A	ENSP00000383363.1:p.Asp390Asn
ENST00000400521.6:c.1171G>A	ENSP00000383365.1:p.Asp391Asn
ENST00000400525.6:c.1102G>A	ENSP00000383369.3:p.Asp368Asn
ENST00000462330.5:c.94G>A	ENSP00000485603.2:p.Asp32Asn
ENST00000462843.2:c.121G>A	ENSP00000485466.2:p.Asp41Asn
ENST00000474308.5:c.1114G>A	ENSP00000485665.1:p.Asp372Asn
ENST00000485358.5:c.139G>A	ENSP00000485499.2:p.Asp47Asn
ENST00000487165.5:n.1265G>A
ENST00000494454.5:n.1245G>A
ENST00000495655.2:n.715G>A
ENST00000542719.6:c.883G>A	ENSP00000485128.2:p.Asp295Asn
ENST00000634471.1:n.244-362G>A
ENST00000634537.1:c.400G>A	ENSP00000489208.1:p.Asp134Asn
NM_006440.4:c.1171G>A	NP_006431.2:p.Asp391Asn
NM_001352300.1:c.1168G>A	NP_001339229.1:p.Asp390Asn
NM_001352301.1:c.1081G>A	NP_001339230.1:p.Asp361Asn
NM_001352302.1:c.883G>A	NP_001339231.1:p.Asp295Asn
NR_147957.1:n.1303G>A
NM_006440.5:c.1171G>A MANE Select	NP_006431.2:p.Asp391Asn
NM_001352300.2:c.1168G>A	NP_001339229.1:p.Asp390Asn
NR_147957.2:n.1129G>A
NM_001352301.2:c.1081G>A	NP_001339230.1:p.Asp361Asn
NM_001352302.2:c.883G>A	NP_001339231.1:p.Asp295Asn