Canonical Allele Identifier: CA410681927

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868167G>C (hg19) ; chr22:g.19880644G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880644G>C , CM000684.2:g.19880644G>C	GRCh38
NC_000022.10:g.19868167G>C , CM000684.1:g.19868167G>C	GRCh37
NC_000022.9:g.18248167G>C	NCBI36
NG_011835.1:g.66193C>G , LRG_417:g.66193C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1160C>G MANE Select	ENSP00000383365.1:p.Ser387Ter
ENST00000400518.5:c.1070C>G	ENSP00000383362.1:p.Ser357Ter
ENST00000400519.6:c.1157C>G	ENSP00000383363.1:p.Ser386Ter
ENST00000400521.6:c.1160C>G	ENSP00000383365.1:p.Ser387Ter
ENST00000400525.6:c.1091C>G	ENSP00000383369.3:p.Ser364Ter
ENST00000462330.5:c.83C>G	ENSP00000485603.2:p.Ser28Ter
ENST00000462843.2:c.110C>G	ENSP00000485466.2:p.Ser37Ter
ENST00000474308.5:c.1103C>G	ENSP00000485665.1:p.Ser368Ter
ENST00000485358.5:c.128C>G	ENSP00000485499.2:p.Ser43Ter
ENST00000487165.5:n.1254C>G
ENST00000494454.5:n.1234C>G
ENST00000495655.2:n.704C>G
ENST00000542719.6:c.872C>G	ENSP00000485128.2:p.Ser291Ter
ENST00000634471.1:n.244-373C>G
ENST00000634537.1:c.389C>G	ENSP00000489208.1:p.Ser130Ter
NM_006440.4:c.1160C>G	NP_006431.2:p.Ser387Ter
NM_001352300.1:c.1157C>G	NP_001339229.1:p.Ser386Ter
NM_001352301.1:c.1070C>G	NP_001339230.1:p.Ser357Ter
NM_001352302.1:c.872C>G	NP_001339231.1:p.Ser291Ter
NR_147957.1:n.1292C>G
NM_006440.5:c.1160C>G MANE Select	NP_006431.2:p.Ser387Ter
NM_001352300.2:c.1157C>G	NP_001339229.1:p.Ser386Ter
NR_147957.2:n.1118C>G
NM_001352301.2:c.1070C>G	NP_001339230.1:p.Ser357Ter
NM_001352302.2:c.872C>G	NP_001339231.1:p.Ser291Ter