Canonical Allele Identifier: CA2655329149

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918728-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918728G>T , CM000684.2:g.19918728G>T	GRCh38
NC_000022.10:g.19906251G>T , CM000684.1:g.19906251G>T	GRCh37
NC_000022.9:g.18286251G>T	NCBI36
NG_011835.1:g.28109C>A , LRG_417:g.28109C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.374+132C>A MANE Select	ENSP00000383365.1:n.374+132C>A
ENST00000334363.14:c.374+132C>A	ENSP00000334451.9:n.374+132C>A
ENST00000400518.5:c.284+132C>A	ENSP00000383362.1:n.284+132C>A
ENST00000400519.6:c.371+132C>A	ENSP00000383363.1:n.371+132C>A
ENST00000400521.6:c.374+132C>A	ENSP00000383365.1:n.374+132C>A
ENST00000400525.6:c.305+132C>A	ENSP00000383369.3:n.305+132C>A
ENST00000474308.5:c.317+132C>A	ENSP00000485665.1:n.317+132C>A
ENST00000491939.6:c.278+132C>A	ENSP00000485543.1:n.278+132C>A
ENST00000496729.2:n.379+132C>A
ENST00000542719.6:c.86+132C>A	ENSP00000485128.2:n.86+132C>A
NM_001282512.1:c.374+132C>A	NP_001269441.1:n.374+132C>A
NM_006440.4:c.374+132C>A	NP_006431.2:n.374+132C>A
NM_001282512.2:c.374+132C>A	NP_001269441.1:n.374+132C>A
NM_001352300.1:c.371+132C>A	NP_001339229.1:n.371+132C>A
NM_001352301.1:c.284+132C>A	NP_001339230.1:n.284+132C>A
NM_001352302.1:c.86+132C>A	NP_001339231.1:n.86+132C>A
NM_001352303.1:c.278+132C>A	NP_001339232.1:n.278+132C>A
NR_147957.1:n.506+132C>A
NM_006440.5:c.374+132C>A MANE Select	NP_006431.2:n.374+132C>A
NM_001282512.3:c.374+132C>A	NP_001269441.1:n.374+132C>A
NM_001352300.2:c.371+132C>A	NP_001339229.1:n.371+132C>A
NR_147957.2:n.332+132C>A
NM_001352301.2:c.284+132C>A	NP_001339230.1:n.284+132C>A
NM_001352302.2:c.86+132C>A	NP_001339231.1:n.86+132C>A
NM_001352303.2:c.278+132C>A	NP_001339232.1:n.278+132C>A