Canonical Allele Identifier: CA410693908

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906467A>G (hg19) ; chr22:g.19918944A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918944A>G , CM000684.2:g.19918944A>G	GRCh38
NC_000022.10:g.19906467A>G , CM000684.1:g.19906467A>G	GRCh37
NC_000022.9:g.18286467A>G	NCBI36
NG_011835.1:g.27893T>C , LRG_417:g.27893T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.290T>C MANE Select	ENSP00000383365.1:p.Met97Thr
ENST00000334363.14:c.290T>C	ENSP00000334451.9:p.Met97Thr
ENST00000400518.5:c.200T>C	ENSP00000383362.1:p.Met67Thr
ENST00000400519.6:c.287T>C	ENSP00000383363.1:p.Met96Thr
ENST00000400521.6:c.290T>C	ENSP00000383365.1:p.Met97Thr
ENST00000400525.6:c.221T>C	ENSP00000383369.3:p.Met74Thr
ENST00000474308.5:c.233T>C	ENSP00000485665.1:p.Met78Thr
ENST00000491939.6:c.194T>C	ENSP00000485543.1:p.Met65Thr
ENST00000496729.2:n.295T>C
ENST00000542719.6:c.2T>C	ENSP00000485128.2:p.Met1Thr
NM_001282512.1:c.290T>C	NP_001269441.1:p.Met97Thr
NM_006440.4:c.290T>C	NP_006431.2:p.Met97Thr
NM_001282512.2:c.290T>C	NP_001269441.1:p.Met97Thr
NM_001352300.1:c.287T>C	NP_001339229.1:p.Met96Thr
NM_001352301.1:c.200T>C	NP_001339230.1:p.Met67Thr
NM_001352302.1:c.2T>C	NP_001339231.1:p.Met1Thr
NM_001352303.1:c.194T>C	NP_001339232.1:p.Met65Thr
NR_147957.1:n.422T>C
NM_006440.5:c.290T>C MANE Select	NP_006431.2:p.Met97Thr
NM_001282512.3:c.290T>C	NP_001269441.1:p.Met97Thr
NM_001352300.2:c.287T>C	NP_001339229.1:p.Met96Thr
NR_147957.2:n.248T>C
NM_001352301.2:c.200T>C	NP_001339230.1:p.Met67Thr
NM_001352302.2:c.2T>C	NP_001339231.1:p.Met1Thr
NM_001352303.2:c.194T>C	NP_001339232.1:p.Met65Thr