Canonical Allele Identifier: CA410681976

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868195G>C (hg19) ; chr22:g.19880672G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880672G>C , CM000684.2:g.19880672G>C	GRCh38
NC_000022.10:g.19868195G>C , CM000684.1:g.19868195G>C	GRCh37
NC_000022.9:g.18248195G>C	NCBI36
NG_011835.1:g.66165C>G , LRG_417:g.66165C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1132C>G MANE Select	ENSP00000383365.1:p.Leu378Val
ENST00000400518.5:c.1042C>G	ENSP00000383362.1:p.Leu348Val
ENST00000400519.6:c.1129C>G	ENSP00000383363.1:p.Leu377Val
ENST00000400521.6:c.1132C>G	ENSP00000383365.1:p.Leu378Val
ENST00000400525.6:c.1063C>G	ENSP00000383369.3:p.Leu355Val
ENST00000462330.5:c.55C>G	ENSP00000485603.2:p.Leu19Val
ENST00000462843.2:c.82C>G	ENSP00000485466.2:p.Leu28Val
ENST00000474308.5:c.1075C>G	ENSP00000485665.1:p.Leu359Val
ENST00000485358.5:c.100C>G	ENSP00000485499.2:p.Leu34Val
ENST00000487165.5:n.1226C>G
ENST00000494454.5:n.1206C>G
ENST00000495655.2:n.676C>G
ENST00000542719.6:c.844C>G	ENSP00000485128.2:p.Leu282Val
ENST00000634471.1:n.244-401C>G
ENST00000634537.1:c.361C>G	ENSP00000489208.1:p.Leu121Val
NM_006440.4:c.1132C>G	NP_006431.2:p.Leu378Val
NM_001352300.1:c.1129C>G	NP_001339229.1:p.Leu377Val
NM_001352301.1:c.1042C>G	NP_001339230.1:p.Leu348Val
NM_001352302.1:c.844C>G	NP_001339231.1:p.Leu282Val
NR_147957.1:n.1264C>G
NM_006440.5:c.1132C>G MANE Select	NP_006431.2:p.Leu378Val
NM_001352300.2:c.1129C>G	NP_001339229.1:p.Leu377Val
NR_147957.2:n.1090C>G
NM_001352301.2:c.1042C>G	NP_001339230.1:p.Leu348Val
NM_001352302.2:c.844C>G	NP_001339231.1:p.Leu282Val