Canonical Allele Identifier: CA513361659

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868217T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880694T>G , CM000684.2:g.19880694T>G	GRCh38
NC_000022.10:g.19868217T>G , CM000684.1:g.19868217T>G	GRCh37
NC_000022.9:g.18248217T>G	NCBI36
NG_011835.1:g.66143A>C , LRG_417:g.66143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1110A>C MANE Select	ENSP00000383365.1:p.Ile370=
ENST00000400518.5:c.1020A>C	ENSP00000383362.1:p.Ile340=
ENST00000400519.6:c.1107A>C	ENSP00000383363.1:p.Ile369=
ENST00000400521.6:c.1110A>C	ENSP00000383365.1:p.Ile370=
ENST00000400525.6:c.1041A>C	ENSP00000383369.3:p.Ile347=
ENST00000462330.5:c.33A>C	ENSP00000485603.2:p.Ile11=
ENST00000462843.2:c.60A>C	ENSP00000485466.2:p.Ile20=
ENST00000474308.5:c.1053A>C	ENSP00000485665.1:p.Ile351=
ENST00000485358.5:c.78A>C	ENSP00000485499.2:p.Ile26=
ENST00000487165.5:n.1204A>C
ENST00000494454.5:n.1184A>C
ENST00000495655.2:n.654A>C
ENST00000542719.6:c.822A>C	ENSP00000485128.2:p.Ile274=
ENST00000634471.1:n.244-423A>C
ENST00000634537.1:c.339A>C	ENSP00000489208.1:p.Ile113=
NM_006440.4:c.1110A>C	NP_006431.2:p.Ile370=
NM_001352300.1:c.1107A>C	NP_001339229.1:p.Ile369=
NM_001352301.1:c.1020A>C	NP_001339230.1:p.Ile340=
NM_001352302.1:c.822A>C	NP_001339231.1:p.Ile274=
NR_147957.1:n.1242A>C
NM_006440.5:c.1110A>C MANE Select	NP_006431.2:p.Ile370=
NM_001352300.2:c.1107A>C	NP_001339229.1:p.Ile369=
NR_147957.2:n.1068A>C
NM_001352301.2:c.1020A>C	NP_001339230.1:p.Ile340=
NM_001352302.2:c.822A>C	NP_001339231.1:p.Ile274=