Canonical Allele Identifier: CA2655329354

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918900-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918903_19918905del , CM000684.2:g.19918903_19918905del	GRCh38
NC_000022.10:g.19906426_19906428del , CM000684.1:g.19906426_19906428del	GRCh37
NC_000022.9:g.18286426_18286428del	NCBI36
NG_011835.1:g.27934_27936del , LRG_417:g.27934_27936del

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.331_333del MANE Select	ENSP00000383365.1:p.Pro111del
ENST00000334363.14:c.331_333del	ENSP00000334451.9:p.Pro111del
ENST00000400518.5:c.241_243del	ENSP00000383362.1:p.Pro81del
ENST00000400519.6:c.328_330del	ENSP00000383363.1:p.Pro110del
ENST00000400521.6:c.331_333del	ENSP00000383365.1:p.Pro111del
ENST00000400525.6:c.262_264del	ENSP00000383369.3:p.Pro88del
ENST00000474308.5:c.274_276del	ENSP00000485665.1:p.Pro92del
ENST00000491939.6:c.235_237del	ENSP00000485543.1:p.Pro79del
ENST00000496729.2:n.336_338del
ENST00000542719.6:c.43_45del	ENSP00000485128.2:p.Pro15del
NM_001282512.1:c.331_333del	NP_001269441.1:p.Pro111del
NM_006440.4:c.331_333del	NP_006431.2:p.Pro111del
NM_001282512.2:c.331_333del	NP_001269441.1:p.Pro111del
NM_001352300.1:c.328_330del	NP_001339229.1:p.Pro110del
NM_001352301.1:c.241_243del	NP_001339230.1:p.Pro81del
NM_001352302.1:c.43_45del	NP_001339231.1:p.Pro15del
NM_001352303.1:c.235_237del	NP_001339232.1:p.Pro79del
NR_147957.1:n.463_465del
NM_006440.5:c.331_333del MANE Select	NP_006431.2:p.Pro111del
NM_001282512.3:c.331_333del	NP_001269441.1:p.Pro111del
NM_001352300.2:c.328_330del	NP_001339229.1:p.Pro110del
NR_147957.2:n.289_291del
NM_001352301.2:c.241_243del	NP_001339230.1:p.Pro81del
NM_001352302.2:c.43_45del	NP_001339231.1:p.Pro15del
NM_001352303.2:c.235_237del	NP_001339232.1:p.Pro79del