Canonical Allele Identifier: CA410693718

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906413C>G (hg19) ; chr22:g.19918890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918890C>G , CM000684.2:g.19918890C>G	GRCh38
NC_000022.10:g.19906413C>G , CM000684.1:g.19906413C>G	GRCh37
NC_000022.9:g.18286413C>G	NCBI36
NG_011835.1:g.27947G>C , LRG_417:g.27947G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.344G>C MANE Select	ENSP00000383365.1:p.Trp115Ser
ENST00000334363.14:c.344G>C	ENSP00000334451.9:p.Trp115Ser
ENST00000400518.5:c.254G>C	ENSP00000383362.1:p.Trp85Ser
ENST00000400519.6:c.341G>C	ENSP00000383363.1:p.Trp114Ser
ENST00000400521.6:c.344G>C	ENSP00000383365.1:p.Trp115Ser
ENST00000400525.6:c.275G>C	ENSP00000383369.3:p.Trp92Ser
ENST00000474308.5:c.287G>C	ENSP00000485665.1:p.Trp96Ser
ENST00000491939.6:c.248G>C	ENSP00000485543.1:p.Trp83Ser
ENST00000496729.2:n.349G>C
ENST00000542719.6:c.56G>C	ENSP00000485128.2:p.Trp19Ser
NM_001282512.1:c.344G>C	NP_001269441.1:p.Trp115Ser
NM_006440.4:c.344G>C	NP_006431.2:p.Trp115Ser
NM_001282512.2:c.344G>C	NP_001269441.1:p.Trp115Ser
NM_001352300.1:c.341G>C	NP_001339229.1:p.Trp114Ser
NM_001352301.1:c.254G>C	NP_001339230.1:p.Trp85Ser
NM_001352302.1:c.56G>C	NP_001339231.1:p.Trp19Ser
NM_001352303.1:c.248G>C	NP_001339232.1:p.Trp83Ser
NR_147957.1:n.476G>C
NM_006440.5:c.344G>C MANE Select	NP_006431.2:p.Trp115Ser
NM_001282512.3:c.344G>C	NP_001269441.1:p.Trp115Ser
NM_001352300.2:c.341G>C	NP_001339229.1:p.Trp114Ser
NR_147957.2:n.302G>C
NM_001352301.2:c.254G>C	NP_001339230.1:p.Trp85Ser
NM_001352302.2:c.56G>C	NP_001339231.1:p.Trp19Ser
NM_001352303.2:c.248G>C	NP_001339232.1:p.Trp83Ser