Canonical Allele Identifier: CA513365397

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883053G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895530G>A , CM000684.2:g.19895530G>A	GRCh38
NC_000022.10:g.19883053G>A , CM000684.1:g.19883053G>A	GRCh37
NC_000022.9:g.18263053G>A	NCBI36
NG_011835.1:g.51307C>T , LRG_417:g.51307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.826C>T MANE Select	ENSP00000383365.1:p.Leu276=
ENST00000334363.14:c.826C>T	ENSP00000334451.9:p.Leu276=
ENST00000400518.5:c.736C>T	ENSP00000383362.1:p.Leu246=
ENST00000400519.6:c.823C>T	ENSP00000383363.1:p.Leu275=
ENST00000400521.6:c.826C>T	ENSP00000383365.1:p.Leu276=
ENST00000400525.6:c.757C>T	ENSP00000383369.3:p.Leu253=
ENST00000474308.5:c.769C>T	ENSP00000485665.1:p.Leu257=
ENST00000475995.3:c.323C>T
ENST00000491939.6:c.730C>T	ENSP00000485543.1:p.Leu244=
ENST00000494454.5:n.900C>T
ENST00000542719.6:c.538C>T	ENSP00000485128.2:p.Leu180=
ENST00000634537.1:c.55C>T	ENSP00000489208.1:p.Leu19=
ENST00000635155.1:n.412C>T
NM_001282512.1:c.826C>T	NP_001269441.1:p.Leu276=
NM_006440.4:c.826C>T	NP_006431.2:p.Leu276=
NM_001282512.2:c.826C>T	NP_001269441.1:p.Leu276=
NM_001352300.1:c.823C>T	NP_001339229.1:p.Leu275=
NM_001352301.1:c.736C>T	NP_001339230.1:p.Leu246=
NM_001352302.1:c.538C>T	NP_001339231.1:p.Leu180=
NM_001352303.1:c.730C>T	NP_001339232.1:p.Leu244=
NR_147957.1:n.958C>T
NM_006440.5:c.826C>T MANE Select	NP_006431.2:p.Leu276=
NM_001282512.3:c.826C>T	NP_001269441.1:p.Leu276=
NM_001352300.2:c.823C>T	NP_001339229.1:p.Leu275=
NR_147957.2:n.784C>T
NM_001352301.2:c.736C>T	NP_001339230.1:p.Leu246=
NM_001352302.2:c.538C>T	NP_001339231.1:p.Leu180=
NM_001352303.2:c.730C>T	NP_001339232.1:p.Leu244=