Canonical Allele Identifier: CA410686654

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883038G>T (hg19) ; chr22:g.19895515G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895515G>T , CM000684.2:g.19895515G>T	GRCh38
NC_000022.10:g.19883038G>T , CM000684.1:g.19883038G>T	GRCh37
NC_000022.9:g.18263038G>T	NCBI36
NG_011835.1:g.51322C>A , LRG_417:g.51322C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.841C>A MANE Select	ENSP00000383365.1:p.Pro281Thr
ENST00000334363.14:c.841C>A	ENSP00000334451.9:p.Pro281Thr
ENST00000400518.5:c.751C>A	ENSP00000383362.1:p.Pro251Thr
ENST00000400519.6:c.838C>A	ENSP00000383363.1:p.Pro280Thr
ENST00000400521.6:c.841C>A	ENSP00000383365.1:p.Pro281Thr
ENST00000400525.6:c.772C>A	ENSP00000383369.3:p.Pro258Thr
ENST00000474308.5:c.784C>A	ENSP00000485665.1:p.Pro262Thr
ENST00000475995.3:c.338C>A
ENST00000491939.6:c.745C>A	ENSP00000485543.1:p.Pro249Thr
ENST00000494454.5:n.915C>A
ENST00000542719.6:c.553C>A	ENSP00000485128.2:p.Pro185Thr
ENST00000634537.1:c.70C>A	ENSP00000489208.1:p.Pro24Thr
ENST00000635155.1:n.427C>A
NM_001282512.1:c.841C>A	NP_001269441.1:p.Pro281Thr
NM_006440.4:c.841C>A	NP_006431.2:p.Pro281Thr
NM_001282512.2:c.841C>A	NP_001269441.1:p.Pro281Thr
NM_001352300.1:c.838C>A	NP_001339229.1:p.Pro280Thr
NM_001352301.1:c.751C>A	NP_001339230.1:p.Pro251Thr
NM_001352302.1:c.553C>A	NP_001339231.1:p.Pro185Thr
NM_001352303.1:c.745C>A	NP_001339232.1:p.Pro249Thr
NR_147957.1:n.973C>A
NM_006440.5:c.841C>A MANE Select	NP_006431.2:p.Pro281Thr
NM_001282512.3:c.841C>A	NP_001269441.1:p.Pro281Thr
NM_001352300.2:c.838C>A	NP_001339229.1:p.Pro280Thr
NR_147957.2:n.799C>A
NM_001352301.2:c.751C>A	NP_001339230.1:p.Pro251Thr
NM_001352302.2:c.553C>A	NP_001339231.1:p.Pro185Thr
NM_001352303.2:c.745C>A	NP_001339232.1:p.Pro249Thr