Canonical Allele Identifier: CA513361647

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880673-G-T
• MyVariant Identifiers: chr22:g.19868196G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880673G>T , CM000684.2:g.19880673G>T	GRCh38
NC_000022.10:g.19868196G>T , CM000684.1:g.19868196G>T	GRCh37
NC_000022.9:g.18248196G>T	NCBI36
NG_011835.1:g.66164C>A , LRG_417:g.66164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1131C>A MANE Select	ENSP00000383365.1:p.Leu377=
ENST00000400518.5:c.1041C>A	ENSP00000383362.1:p.Leu347=
ENST00000400519.6:c.1128C>A	ENSP00000383363.1:p.Leu376=
ENST00000400521.6:c.1131C>A	ENSP00000383365.1:p.Leu377=
ENST00000400525.6:c.1062C>A	ENSP00000383369.3:p.Leu354=
ENST00000462330.5:c.54C>A	ENSP00000485603.2:p.Leu18=
ENST00000462843.2:c.81C>A	ENSP00000485466.2:p.Leu27=
ENST00000474308.5:c.1074C>A	ENSP00000485665.1:p.Leu358=
ENST00000485358.5:c.99C>A	ENSP00000485499.2:p.Leu33=
ENST00000487165.5:n.1225C>A
ENST00000494454.5:n.1205C>A
ENST00000495655.2:n.675C>A
ENST00000542719.6:c.843C>A	ENSP00000485128.2:p.Leu281=
ENST00000634471.1:n.244-402C>A
ENST00000634537.1:c.360C>A	ENSP00000489208.1:p.Leu120=
NM_006440.4:c.1131C>A	NP_006431.2:p.Leu377=
NM_001352300.1:c.1128C>A	NP_001339229.1:p.Leu376=
NM_001352301.1:c.1041C>A	NP_001339230.1:p.Leu347=
NM_001352302.1:c.843C>A	NP_001339231.1:p.Leu281=
NR_147957.1:n.1263C>A
NM_006440.5:c.1131C>A MANE Select	NP_006431.2:p.Leu377=
NM_001352300.2:c.1128C>A	NP_001339229.1:p.Leu376=
NR_147957.2:n.1089C>A
NM_001352301.2:c.1041C>A	NP_001339230.1:p.Leu347=
NM_001352302.2:c.843C>A	NP_001339231.1:p.Leu281=