Canonical Allele Identifier: CA410682015

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868215G>C (hg19) ; chr22:g.19880692G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880692G>C , CM000684.2:g.19880692G>C	GRCh38
NC_000022.10:g.19868215G>C , CM000684.1:g.19868215G>C	GRCh37
NC_000022.9:g.18248215G>C	NCBI36
NG_011835.1:g.66145C>G , LRG_417:g.66145C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1112C>G MANE Select	ENSP00000383365.1:p.Ala371Gly
ENST00000400518.5:c.1022C>G	ENSP00000383362.1:p.Ala341Gly
ENST00000400519.6:c.1109C>G	ENSP00000383363.1:p.Ala370Gly
ENST00000400521.6:c.1112C>G	ENSP00000383365.1:p.Ala371Gly
ENST00000400525.6:c.1043C>G	ENSP00000383369.3:p.Ala348Gly
ENST00000462330.5:c.35C>G	ENSP00000485603.2:p.Ala12Gly
ENST00000462843.2:c.62C>G	ENSP00000485466.2:p.Ala21Gly
ENST00000474308.5:c.1055C>G	ENSP00000485665.1:p.Ala352Gly
ENST00000485358.5:c.80C>G	ENSP00000485499.2:p.Ala27Gly
ENST00000487165.5:n.1206C>G
ENST00000494454.5:n.1186C>G
ENST00000495655.2:n.656C>G
ENST00000542719.6:c.824C>G	ENSP00000485128.2:p.Ala275Gly
ENST00000634471.1:n.244-421C>G
ENST00000634537.1:c.341C>G	ENSP00000489208.1:p.Ala114Gly
NM_006440.4:c.1112C>G	NP_006431.2:p.Ala371Gly
NM_001352300.1:c.1109C>G	NP_001339229.1:p.Ala370Gly
NM_001352301.1:c.1022C>G	NP_001339230.1:p.Ala341Gly
NM_001352302.1:c.824C>G	NP_001339231.1:p.Ala275Gly
NR_147957.1:n.1244C>G
NM_006440.5:c.1112C>G MANE Select	NP_006431.2:p.Ala371Gly
NM_001352300.2:c.1109C>G	NP_001339229.1:p.Ala370Gly
NR_147957.2:n.1070C>G
NM_001352301.2:c.1022C>G	NP_001339230.1:p.Ala341Gly
NM_001352302.2:c.824C>G	NP_001339231.1:p.Ala275Gly