Canonical Allele Identifier: CA10103803

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880695A>G , CM000684.2:g.19880695A>G	GRCh38
NC_000022.10:g.19868218A>G , CM000684.1:g.19868218A>G	GRCh37
NC_000022.9:g.18248218A>G	NCBI36
NG_011835.1:g.66142T>C , LRG_417:g.66142T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1109T>C MANE Select	ENSP00000383365.1:p.Ile370Thr
ENST00000400518.5:c.1019T>C	ENSP00000383362.1:p.Ile340Thr
ENST00000400519.6:c.1106T>C	ENSP00000383363.1:p.Ile369Thr
ENST00000400521.6:c.1109T>C	ENSP00000383365.1:p.Ile370Thr
ENST00000400525.6:c.1040T>C	ENSP00000383369.3:p.Ile347Thr
ENST00000462330.5:c.32T>C	ENSP00000485603.2:p.Ile11Thr
ENST00000462843.2:c.59T>C	ENSP00000485466.2:p.Ile20Thr
ENST00000474308.5:c.1052T>C	ENSP00000485665.1:p.Ile351Thr
ENST00000485358.5:c.77T>C	ENSP00000485499.2:p.Ile26Thr
ENST00000487165.5:n.1203T>C
ENST00000494454.5:n.1183T>C
ENST00000495655.2:n.653T>C
ENST00000542719.6:c.821T>C	ENSP00000485128.2:p.Ile274Thr
ENST00000634471.1:n.244-424T>C
ENST00000634537.1:c.338T>C	ENSP00000489208.1:p.Ile113Thr
NM_006440.4:c.1109T>C	NP_006431.2:p.Ile370Thr
NM_001352300.1:c.1106T>C	NP_001339229.1:p.Ile369Thr
NM_001352301.1:c.1019T>C	NP_001339230.1:p.Ile340Thr
NM_001352302.1:c.821T>C	NP_001339231.1:p.Ile274Thr
NR_147957.1:n.1241T>C
NM_006440.5:c.1109T>C MANE Select	NP_006431.2:p.Ile370Thr
NM_001352300.2:c.1106T>C	NP_001339229.1:p.Ile369Thr
NR_147957.2:n.1067T>C
NM_001352301.2:c.1019T>C	NP_001339230.1:p.Ile340Thr
NM_001352302.2:c.821T>C	NP_001339231.1:p.Ile274Thr