Canonical Allele Identifier: CA513361618

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868162G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1165C>T MANE Select	ENSP00000383365.1:p.Leu389=
ENST00000400518.5:c.1075C>T	ENSP00000383362.1:p.Leu359=
ENST00000400519.6:c.1162C>T	ENSP00000383363.1:p.Leu388=
ENST00000400521.6:c.1165C>T	ENSP00000383365.1:p.Leu389=
ENST00000400525.6:c.1096C>T	ENSP00000383369.3:p.Leu366=
ENST00000462330.5:c.88C>T	ENSP00000485603.2:p.Leu30=
ENST00000462843.2:c.115C>T	ENSP00000485466.2:p.Leu39=
ENST00000474308.5:c.1108C>T	ENSP00000485665.1:p.Leu370=
ENST00000485358.5:c.133C>T	ENSP00000485499.2:p.Leu45=
ENST00000487165.5:n.1259C>T
ENST00000494454.5:n.1239C>T
ENST00000495655.2:n.709C>T
ENST00000542719.6:c.877C>T	ENSP00000485128.2:p.Leu293=
ENST00000634471.1:n.244-368C>T
ENST00000634537.1:c.394C>T	ENSP00000489208.1:p.Leu132=
NM_006440.4:c.1165C>T	NP_006431.2:p.Leu389=
NM_001352300.1:c.1162C>T	NP_001339229.1:p.Leu388=
NM_001352301.1:c.1075C>T	NP_001339230.1:p.Leu359=
NM_001352302.1:c.877C>T	NP_001339231.1:p.Leu293=
NR_147957.1:n.1297C>T
NM_006440.5:c.1165C>T MANE Select	NP_006431.2:p.Leu389=
NM_001352300.2:c.1162C>T	NP_001339229.1:p.Leu388=
NR_147957.2:n.1123C>T
NM_001352301.2:c.1075C>T	NP_001339230.1:p.Leu359=
NM_001352302.2:c.877C>T	NP_001339231.1:p.Leu293=