Canonical Allele Identifier: CA410681917

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868162G>T (hg19) ; chr22:g.19880639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880639G>T , CM000684.2:g.19880639G>T	GRCh38
NC_000022.10:g.19868162G>T , CM000684.1:g.19868162G>T	GRCh37
NC_000022.9:g.18248162G>T	NCBI36
NG_011835.1:g.66198C>A , LRG_417:g.66198C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1165C>A MANE Select	ENSP00000383365.1:p.Leu389Met
ENST00000400518.5:c.1075C>A	ENSP00000383362.1:p.Leu359Met
ENST00000400519.6:c.1162C>A	ENSP00000383363.1:p.Leu388Met
ENST00000400521.6:c.1165C>A	ENSP00000383365.1:p.Leu389Met
ENST00000400525.6:c.1096C>A	ENSP00000383369.3:p.Leu366Met
ENST00000462330.5:c.88C>A	ENSP00000485603.2:p.Leu30Met
ENST00000462843.2:c.115C>A	ENSP00000485466.2:p.Leu39Met
ENST00000474308.5:c.1108C>A	ENSP00000485665.1:p.Leu370Met
ENST00000485358.5:c.133C>A	ENSP00000485499.2:p.Leu45Met
ENST00000487165.5:n.1259C>A
ENST00000494454.5:n.1239C>A
ENST00000495655.2:n.709C>A
ENST00000542719.6:c.877C>A	ENSP00000485128.2:p.Leu293Met
ENST00000634471.1:n.244-368C>A
ENST00000634537.1:c.394C>A	ENSP00000489208.1:p.Leu132Met
NM_006440.4:c.1165C>A	NP_006431.2:p.Leu389Met
NM_001352300.1:c.1162C>A	NP_001339229.1:p.Leu388Met
NM_001352301.1:c.1075C>A	NP_001339230.1:p.Leu359Met
NM_001352302.1:c.877C>A	NP_001339231.1:p.Leu293Met
NR_147957.1:n.1297C>A
NM_006440.5:c.1165C>A MANE Select	NP_006431.2:p.Leu389Met
NM_001352300.2:c.1162C>A	NP_001339229.1:p.Leu388Met
NR_147957.2:n.1123C>A
NM_001352301.2:c.1075C>A	NP_001339230.1:p.Leu359Met
NM_001352302.2:c.877C>A	NP_001339231.1:p.Leu293Met