Canonical Allele Identifier: CA513369123

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19919003-G-T
• MyVariant Identifiers: chr22:g.19906526G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919003G>T , CM000684.2:g.19919003G>T	GRCh38
NC_000022.10:g.19906526G>T , CM000684.1:g.19906526G>T	GRCh37
NC_000022.9:g.18286526G>T	NCBI36
NG_011835.1:g.27834C>A , LRG_417:g.27834C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.231C>A MANE Select	ENSP00000383365.1:p.Gly77=
ENST00000334363.14:c.231C>A	ENSP00000334451.9:p.Gly77=
ENST00000400518.5:c.141C>A	ENSP00000383362.1:p.Gly47=
ENST00000400519.6:c.228C>A	ENSP00000383363.1:p.Gly76=
ENST00000400521.6:c.231C>A	ENSP00000383365.1:p.Gly77=
ENST00000400525.6:c.162C>A	ENSP00000383369.3:p.Gly54=
ENST00000474308.5:c.174C>A	ENSP00000485665.1:p.Gly58=
ENST00000491939.6:c.135C>A	ENSP00000485543.1:p.Gly45=
ENST00000496729.2:n.236C>A
ENST00000542719.6:c.-58C>A	ENSP00000485128.2:n.-58C>A
NM_001282512.1:c.231C>A	NP_001269441.1:p.Gly77=
NM_006440.4:c.231C>A	NP_006431.2:p.Gly77=
NM_001282512.2:c.231C>A	NP_001269441.1:p.Gly77=
NM_001352300.1:c.228C>A	NP_001339229.1:p.Gly76=
NM_001352301.1:c.141C>A	NP_001339230.1:p.Gly47=
NM_001352302.1:c.-58C>A	NP_001339231.1:n.-58C>A
NM_001352303.1:c.135C>A	NP_001339232.1:p.Gly45=
NR_147957.1:n.363C>A
NM_006440.5:c.231C>A MANE Select	NP_006431.2:p.Gly77=
NM_001282512.3:c.231C>A	NP_001269441.1:p.Gly77=
NM_001352300.2:c.228C>A	NP_001339229.1:p.Gly76=
NR_147957.2:n.189C>A
NM_001352301.2:c.141C>A	NP_001339230.1:p.Gly47=
NM_001352302.2:c.-58C>A	NP_001339231.1:n.-58C>A
NM_001352303.2:c.135C>A	NP_001339232.1:p.Gly45=