Canonical Allele Identifier: CA322091844

Gene: TXNRD2

Linked Data

• dbSNP Id: rs938417099
• MyVariant Identifiers: chr22:g.19867461T>C (hg19) ; chr22:g.19879938T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19879938T>C , CM000684.2:g.19879938T>C	GRCh38
NC_000022.10:g.19867461T>C , CM000684.1:g.19867461T>C	GRCh37
NC_000022.9:g.18247461T>C	NCBI36
NG_011835.1:g.66899A>G , LRG_417:g.66899A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1275+241A>G MANE Select	ENSP00000383365.1:n.1275+241A>G
ENST00000400518.5:c.1185+241A>G	ENSP00000383362.1:n.1185+241A>G
ENST00000400519.6:c.1272+241A>G	ENSP00000383363.1:n.1272+241A>G
ENST00000400521.6:c.1275+241A>G	ENSP00000383365.1:n.1275+241A>G
ENST00000400525.6:c.1206+241A>G	ENSP00000383369.3:n.1206+241A>G
ENST00000462330.5:c.198+241A>G	ENSP00000485603.2:n.198+241A>G
ENST00000462843.2:c.225+241A>G	ENSP00000485466.2:n.225+241A>G
ENST00000474308.5:c.1218+241A>G	ENSP00000485665.1:n.1218+241A>G
ENST00000485358.5:c.243+241A>G	ENSP00000485499.2:n.243+241A>G
ENST00000487165.5:n.1369+241A>G
ENST00000494454.5:n.1349+241A>G
ENST00000495655.2:n.819+241A>G
ENST00000542719.6:c.987+241A>G	ENSP00000485128.2:n.987+241A>G
ENST00000634471.1:n.336+241A>G
ENST00000634537.1:c.504+241A>G	ENSP00000489208.1:n.504+241A>G
NM_006440.4:c.1275+241A>G	NP_006431.2:n.1275+241A>G
NM_001352300.1:c.1272+241A>G	NP_001339229.1:n.1272+241A>G
NM_001352301.1:c.1185+241A>G	NP_001339230.1:n.1185+241A>G
NM_001352302.1:c.987+241A>G	NP_001339231.1:n.987+241A>G
NR_147957.1:n.1407+241A>G
NM_006440.5:c.1275+241A>G MANE Select	NP_006431.2:n.1275+241A>G
NM_001352300.2:c.1272+241A>G	NP_001339229.1:n.1272+241A>G
NR_147957.2:n.1233+241A>G
NM_001352301.2:c.1185+241A>G	NP_001339230.1:n.1185+241A>G
NM_001352302.2:c.987+241A>G	NP_001339231.1:n.987+241A>G