Canonical Allele Identifier: CA410693778

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906430A>C (hg19) ; chr22:g.19918907A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918907A>C , CM000684.2:g.19918907A>C	GRCh38
NC_000022.10:g.19906430A>C , CM000684.1:g.19906430A>C	GRCh37
NC_000022.9:g.18286430A>C	NCBI36
NG_011835.1:g.27930T>G , LRG_417:g.27930T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.327T>G MANE Select	ENSP00000383365.1:p.Asp109Glu
ENST00000334363.14:c.327T>G	ENSP00000334451.9:p.Asp109Glu
ENST00000400518.5:c.237T>G	ENSP00000383362.1:p.Asp79Glu
ENST00000400519.6:c.324T>G	ENSP00000383363.1:p.Asp108Glu
ENST00000400521.6:c.327T>G	ENSP00000383365.1:p.Asp109Glu
ENST00000400525.6:c.258T>G	ENSP00000383369.3:p.Asp86Glu
ENST00000474308.5:c.270T>G	ENSP00000485665.1:p.Asp90Glu
ENST00000491939.6:c.231T>G	ENSP00000485543.1:p.Asp77Glu
ENST00000496729.2:n.332T>G
ENST00000542719.6:c.39T>G	ENSP00000485128.2:p.Asp13Glu
NM_001282512.1:c.327T>G	NP_001269441.1:p.Asp109Glu
NM_006440.4:c.327T>G	NP_006431.2:p.Asp109Glu
NM_001282512.2:c.327T>G	NP_001269441.1:p.Asp109Glu
NM_001352300.1:c.324T>G	NP_001339229.1:p.Asp108Glu
NM_001352301.1:c.237T>G	NP_001339230.1:p.Asp79Glu
NM_001352302.1:c.39T>G	NP_001339231.1:p.Asp13Glu
NM_001352303.1:c.231T>G	NP_001339232.1:p.Asp77Glu
NR_147957.1:n.459T>G
NM_006440.5:c.327T>G MANE Select	NP_006431.2:p.Asp109Glu
NM_001282512.3:c.327T>G	NP_001269441.1:p.Asp109Glu
NM_001352300.2:c.324T>G	NP_001339229.1:p.Asp108Glu
NR_147957.2:n.285T>G
NM_001352301.2:c.237T>G	NP_001339230.1:p.Asp79Glu
NM_001352302.2:c.39T>G	NP_001339231.1:p.Asp13Glu
NM_001352303.2:c.231T>G	NP_001339232.1:p.Asp77Glu