Canonical Allele Identifier: CA410693795

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906434T>G (hg19) ; chr22:g.19918911T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918911T>G , CM000684.2:g.19918911T>G	GRCh38
NC_000022.10:g.19906434T>G , CM000684.1:g.19906434T>G	GRCh37
NC_000022.9:g.18286434T>G	NCBI36
NG_011835.1:g.27926A>C , LRG_417:g.27926A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.323A>C MANE Select	ENSP00000383365.1:p.Gln108Pro
ENST00000334363.14:c.323A>C	ENSP00000334451.9:p.Gln108Pro
ENST00000400518.5:c.233A>C	ENSP00000383362.1:p.Gln78Pro
ENST00000400519.6:c.320A>C	ENSP00000383363.1:p.Gln107Pro
ENST00000400521.6:c.323A>C	ENSP00000383365.1:p.Gln108Pro
ENST00000400525.6:c.254A>C	ENSP00000383369.3:p.Gln85Pro
ENST00000474308.5:c.266A>C	ENSP00000485665.1:p.Gln89Pro
ENST00000491939.6:c.227A>C	ENSP00000485543.1:p.Gln76Pro
ENST00000496729.2:n.328A>C
ENST00000542719.6:c.35A>C	ENSP00000485128.2:p.Gln12Pro
NM_001282512.1:c.323A>C	NP_001269441.1:p.Gln108Pro
NM_006440.4:c.323A>C	NP_006431.2:p.Gln108Pro
NM_001282512.2:c.323A>C	NP_001269441.1:p.Gln108Pro
NM_001352300.1:c.320A>C	NP_001339229.1:p.Gln107Pro
NM_001352301.1:c.233A>C	NP_001339230.1:p.Gln78Pro
NM_001352302.1:c.35A>C	NP_001339231.1:p.Gln12Pro
NM_001352303.1:c.227A>C	NP_001339232.1:p.Gln76Pro
NR_147957.1:n.455A>C
NM_006440.5:c.323A>C MANE Select	NP_006431.2:p.Gln108Pro
NM_001282512.3:c.323A>C	NP_001269441.1:p.Gln108Pro
NM_001352300.2:c.320A>C	NP_001339229.1:p.Gln107Pro
NR_147957.2:n.281A>C
NM_001352301.2:c.233A>C	NP_001339230.1:p.Gln78Pro
NM_001352302.2:c.35A>C	NP_001339231.1:p.Gln12Pro
NM_001352303.2:c.227A>C	NP_001339232.1:p.Gln76Pro