Canonical Allele Identifier: CA410682065

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868234G>A (hg19) ; chr22:g.19880711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880711G>A , CM000684.2:g.19880711G>A	GRCh38
NC_000022.10:g.19868234G>A , CM000684.1:g.19868234G>A	GRCh37
NC_000022.9:g.18248234G>A	NCBI36
NG_011835.1:g.66126C>T , LRG_417:g.66126C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1093C>T MANE Select	ENSP00000383365.1:p.Pro365Ser
ENST00000400518.5:c.1003C>T	ENSP00000383362.1:p.Pro335Ser
ENST00000400519.6:c.1090C>T	ENSP00000383363.1:p.Pro364Ser
ENST00000400521.6:c.1093C>T	ENSP00000383365.1:p.Pro365Ser
ENST00000400525.6:c.1024C>T	ENSP00000383369.3:p.Pro342Ser
ENST00000462330.5:c.16C>T	ENSP00000485603.2:p.Pro6Ser
ENST00000462843.2:c.43C>T	ENSP00000485466.2:p.Pro15Ser
ENST00000474308.5:c.1036C>T	ENSP00000485665.1:p.Pro346Ser
ENST00000485358.5:c.61C>T	ENSP00000485499.2:p.Pro21Ser
ENST00000487165.5:n.1187C>T
ENST00000494454.5:n.1167C>T
ENST00000495655.2:n.637C>T
ENST00000542719.6:c.805C>T	ENSP00000485128.2:p.Pro269Ser
ENST00000634471.1:n.244-440C>T
ENST00000634537.1:c.322C>T	ENSP00000489208.1:p.Pro108Ser
NM_006440.4:c.1093C>T	NP_006431.2:p.Pro365Ser
NM_001352300.1:c.1090C>T	NP_001339229.1:p.Pro364Ser
NM_001352301.1:c.1003C>T	NP_001339230.1:p.Pro335Ser
NM_001352302.1:c.805C>T	NP_001339231.1:p.Pro269Ser
NR_147957.1:n.1225C>T
NM_006440.5:c.1093C>T MANE Select	NP_006431.2:p.Pro365Ser
NM_001352300.2:c.1090C>T	NP_001339229.1:p.Pro364Ser
NR_147957.2:n.1051C>T
NM_001352301.2:c.1003C>T	NP_001339230.1:p.Pro335Ser
NM_001352302.2:c.805C>T	NP_001339231.1:p.Pro269Ser