Canonical Allele Identifier: CA410682087

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868240C>G (hg19) ; chr22:g.19880717C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880717C>G , CM000684.2:g.19880717C>G	GRCh38
NC_000022.10:g.19868240C>G , CM000684.1:g.19868240C>G	GRCh37
NC_000022.9:g.18248240C>G	NCBI36
NG_011835.1:g.66120G>C , LRG_417:g.66120G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1087G>C MANE Select	ENSP00000383365.1:p.Gly363Arg
ENST00000400518.5:c.997G>C	ENSP00000383362.1:p.Gly333Arg
ENST00000400519.6:c.1084G>C	ENSP00000383363.1:p.Gly362Arg
ENST00000400521.6:c.1087G>C	ENSP00000383365.1:p.Gly363Arg
ENST00000400525.6:c.1018G>C	ENSP00000383369.3:p.Gly340Arg
ENST00000462330.5:c.10G>C	ENSP00000485603.2:p.Gly4Arg
ENST00000462843.2:c.37G>C	ENSP00000485466.2:p.Gly13Arg
ENST00000474308.5:c.1030G>C	ENSP00000485665.1:p.Gly344Arg
ENST00000485358.5:c.55G>C	ENSP00000485499.2:p.Gly19Arg
ENST00000487165.5:n.1181G>C
ENST00000494454.5:n.1161G>C
ENST00000495655.2:n.631G>C
ENST00000542719.6:c.799G>C	ENSP00000485128.2:p.Gly267Arg
ENST00000634471.1:n.244-446G>C
ENST00000634537.1:c.316G>C	ENSP00000489208.1:p.Gly106Arg
NM_006440.4:c.1087G>C	NP_006431.2:p.Gly363Arg
NM_001352300.1:c.1084G>C	NP_001339229.1:p.Gly362Arg
NM_001352301.1:c.997G>C	NP_001339230.1:p.Gly333Arg
NM_001352302.1:c.799G>C	NP_001339231.1:p.Gly267Arg
NR_147957.1:n.1219G>C
NM_006440.5:c.1087G>C MANE Select	NP_006431.2:p.Gly363Arg
NM_001352300.2:c.1084G>C	NP_001339229.1:p.Gly362Arg
NR_147957.2:n.1045G>C
NM_001352301.2:c.997G>C	NP_001339230.1:p.Gly333Arg
NM_001352302.2:c.799G>C	NP_001339231.1:p.Gly267Arg