Canonical Allele Identifier: CA751494248

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1389095812
• MyVariant Identifiers: chr22:g.19868256G>C (hg19) ; chr22:g.19880733G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880733G>C , CM000684.2:g.19880733G>C	GRCh38
NC_000022.10:g.19868256G>C , CM000684.1:g.19868256G>C	GRCh37
NC_000022.9:g.18248256G>C	NCBI36
NG_011835.1:g.66104C>G , LRG_417:g.66104C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1087-16C>G MANE Select	ENSP00000383365.1:n.1087-16C>G
ENST00000400518.5:c.997-16C>G	ENSP00000383362.1:n.997-16C>G
ENST00000400519.6:c.1084-16C>G	ENSP00000383363.1:n.1084-16C>G
ENST00000400521.6:c.1087-16C>G	ENSP00000383365.1:n.1087-16C>G
ENST00000400525.6:c.1018-16C>G	ENSP00000383369.3:n.1018-16C>G
ENST00000462330.5:c.10-16C>G	ENSP00000485603.2:n.10-16C>G
ENST00000462843.2:c.37-16C>G	ENSP00000485466.2:n.37-16C>G
ENST00000474308.5:c.1030-16C>G	ENSP00000485665.1:n.1030-16C>G
ENST00000485358.5:c.55-16C>G	ENSP00000485499.2:n.55-16C>G
ENST00000487165.5:n.1181-16C>G
ENST00000494454.5:n.1161-16C>G
ENST00000495655.2:n.615C>G
ENST00000542719.6:c.799-16C>G	ENSP00000485128.2:n.799-16C>G
ENST00000634471.1:n.244-462C>G
ENST00000634537.1:c.316-16C>G	ENSP00000489208.1:n.316-16C>G
NM_006440.4:c.1087-16C>G	NP_006431.2:n.1087-16C>G
NM_001352300.1:c.1084-16C>G	NP_001339229.1:n.1084-16C>G
NM_001352301.1:c.997-16C>G	NP_001339230.1:n.997-16C>G
NM_001352302.1:c.799-16C>G	NP_001339231.1:n.799-16C>G
NR_147957.1:n.1219-16C>G
NM_006440.5:c.1087-16C>G MANE Select	NP_006431.2:n.1087-16C>G
NM_001352300.2:c.1084-16C>G	NP_001339229.1:n.1084-16C>G
NR_147957.2:n.1045-16C>G
NM_001352301.2:c.997-16C>G	NP_001339230.1:n.997-16C>G
NM_001352302.2:c.799-16C>G	NP_001339231.1:n.799-16C>G