Canonical Allele Identifier: CA410681959

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868185C>G (hg19) ; chr22:g.19880662C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880662C>G , CM000684.2:g.19880662C>G	GRCh38
NC_000022.10:g.19868185C>G , CM000684.1:g.19868185C>G	GRCh37
NC_000022.9:g.18248185C>G	NCBI36
NG_011835.1:g.66175G>C , LRG_417:g.66175G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1142G>C MANE Select	ENSP00000383365.1:p.Arg381Pro
ENST00000400518.5:c.1052G>C	ENSP00000383362.1:p.Arg351Pro
ENST00000400519.6:c.1139G>C	ENSP00000383363.1:p.Arg380Pro
ENST00000400521.6:c.1142G>C	ENSP00000383365.1:p.Arg381Pro
ENST00000400525.6:c.1073G>C	ENSP00000383369.3:p.Arg358Pro
ENST00000462330.5:c.65G>C	ENSP00000485603.2:p.Arg22Pro
ENST00000462843.2:c.92G>C	ENSP00000485466.2:p.Arg31Pro
ENST00000474308.5:c.1085G>C	ENSP00000485665.1:p.Arg362Pro
ENST00000485358.5:c.110G>C	ENSP00000485499.2:p.Arg37Pro
ENST00000487165.5:n.1236G>C
ENST00000494454.5:n.1216G>C
ENST00000495655.2:n.686G>C
ENST00000542719.6:c.854G>C	ENSP00000485128.2:p.Arg285Pro
ENST00000634471.1:n.244-391G>C
ENST00000634537.1:c.371G>C	ENSP00000489208.1:p.Arg124Pro
NM_006440.4:c.1142G>C	NP_006431.2:p.Arg381Pro
NM_001352300.1:c.1139G>C	NP_001339229.1:p.Arg380Pro
NM_001352301.1:c.1052G>C	NP_001339230.1:p.Arg351Pro
NM_001352302.1:c.854G>C	NP_001339231.1:p.Arg285Pro
NR_147957.1:n.1274G>C
NM_006440.5:c.1142G>C MANE Select	NP_006431.2:p.Arg381Pro
NM_001352300.2:c.1139G>C	NP_001339229.1:p.Arg380Pro
NR_147957.2:n.1100G>C
NM_001352301.2:c.1052G>C	NP_001339230.1:p.Arg351Pro
NM_001352302.2:c.854G>C	NP_001339231.1:p.Arg285Pro