Canonical Allele Identifier: CA410682041

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868228G>C (hg19) ; chr22:g.19880705G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880705G>C , CM000684.2:g.19880705G>C	GRCh38
NC_000022.10:g.19868228G>C , CM000684.1:g.19868228G>C	GRCh37
NC_000022.9:g.18248228G>C	NCBI36
NG_011835.1:g.66132C>G , LRG_417:g.66132C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1099C>G MANE Select	ENSP00000383365.1:p.Leu367Val
ENST00000400518.5:c.1009C>G	ENSP00000383362.1:p.Leu337Val
ENST00000400519.6:c.1096C>G	ENSP00000383363.1:p.Leu366Val
ENST00000400521.6:c.1099C>G	ENSP00000383365.1:p.Leu367Val
ENST00000400525.6:c.1030C>G	ENSP00000383369.3:p.Leu344Val
ENST00000462330.5:c.22C>G	ENSP00000485603.2:p.Leu8Val
ENST00000462843.2:c.49C>G	ENSP00000485466.2:p.Leu17Val
ENST00000474308.5:c.1042C>G	ENSP00000485665.1:p.Leu348Val
ENST00000485358.5:c.67C>G	ENSP00000485499.2:p.Leu23Val
ENST00000487165.5:n.1193C>G
ENST00000494454.5:n.1173C>G
ENST00000495655.2:n.643C>G
ENST00000542719.6:c.811C>G	ENSP00000485128.2:p.Leu271Val
ENST00000634471.1:n.244-434C>G
ENST00000634537.1:c.328C>G	ENSP00000489208.1:p.Leu110Val
NM_006440.4:c.1099C>G	NP_006431.2:p.Leu367Val
NM_001352300.1:c.1096C>G	NP_001339229.1:p.Leu366Val
NM_001352301.1:c.1009C>G	NP_001339230.1:p.Leu337Val
NM_001352302.1:c.811C>G	NP_001339231.1:p.Leu271Val
NR_147957.1:n.1231C>G
NM_006440.5:c.1099C>G MANE Select	NP_006431.2:p.Leu367Val
NM_001352300.2:c.1096C>G	NP_001339229.1:p.Leu366Val
NR_147957.2:n.1057C>G
NM_001352301.2:c.1009C>G	NP_001339230.1:p.Leu337Val
NM_001352302.2:c.811C>G	NP_001339231.1:p.Leu271Val