Canonical Allele Identifier: CA410681899

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880631-G-T
• MyVariant Identifiers: chr22:g.19868154G>T (hg19) ; chr22:g.19880631G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880631G>T , CM000684.2:g.19880631G>T	GRCh38
NC_000022.10:g.19868154G>T , CM000684.1:g.19868154G>T	GRCh37
NC_000022.9:g.18248154G>T	NCBI36
NG_011835.1:g.66206C>A , LRG_417:g.66206C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1173C>A MANE Select	ENSP00000383365.1:p.Asp391Glu
ENST00000400518.5:c.1083C>A	ENSP00000383362.1:p.Asp361Glu
ENST00000400519.6:c.1170C>A	ENSP00000383363.1:p.Asp390Glu
ENST00000400521.6:c.1173C>A	ENSP00000383365.1:p.Asp391Glu
ENST00000400525.6:c.1104C>A	ENSP00000383369.3:p.Asp368Glu
ENST00000462330.5:c.96C>A	ENSP00000485603.2:p.Asp32Glu
ENST00000462843.2:c.123C>A	ENSP00000485466.2:p.Asp41Glu
ENST00000474308.5:c.1116C>A	ENSP00000485665.1:p.Asp372Glu
ENST00000485358.5:c.141C>A	ENSP00000485499.2:p.Asp47Glu
ENST00000487165.5:n.1267C>A
ENST00000494454.5:n.1247C>A
ENST00000495655.2:n.717C>A
ENST00000542719.6:c.885C>A	ENSP00000485128.2:p.Asp295Glu
ENST00000634471.1:n.244-360C>A
ENST00000634537.1:c.402C>A	ENSP00000489208.1:p.Asp134Glu
NM_006440.4:c.1173C>A	NP_006431.2:p.Asp391Glu
NM_001352300.1:c.1170C>A	NP_001339229.1:p.Asp390Glu
NM_001352301.1:c.1083C>A	NP_001339230.1:p.Asp361Glu
NM_001352302.1:c.885C>A	NP_001339231.1:p.Asp295Glu
NR_147957.1:n.1305C>A
NM_006440.5:c.1173C>A MANE Select	NP_006431.2:p.Asp391Glu
NM_001352300.2:c.1170C>A	NP_001339229.1:p.Asp390Glu
NR_147957.2:n.1131C>A
NM_001352301.2:c.1083C>A	NP_001339230.1:p.Asp361Glu
NM_001352302.2:c.885C>A	NP_001339231.1:p.Asp295Glu