Canonical Allele Identifier: CA410686733

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883076A>T (hg19) ; chr22:g.19895553A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895553A>T , CM000684.2:g.19895553A>T	GRCh38
NC_000022.10:g.19883076A>T , CM000684.1:g.19883076A>T	GRCh37
NC_000022.9:g.18263076A>T	NCBI36
NG_011835.1:g.51284T>A , LRG_417:g.51284T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.803T>A MANE Select	ENSP00000383365.1:p.Met268Lys
ENST00000334363.14:c.803T>A	ENSP00000334451.9:p.Met268Lys
ENST00000400518.5:c.713T>A	ENSP00000383362.1:p.Met238Lys
ENST00000400519.6:c.800T>A	ENSP00000383363.1:p.Met267Lys
ENST00000400521.6:c.803T>A	ENSP00000383365.1:p.Met268Lys
ENST00000400525.6:c.734T>A	ENSP00000383369.3:p.Met245Lys
ENST00000474308.5:c.746T>A	ENSP00000485665.1:p.Met249Lys
ENST00000475995.3:c.300T>A
ENST00000491939.6:c.707T>A	ENSP00000485543.1:p.Met236Lys
ENST00000494454.5:n.877T>A
ENST00000542719.6:c.515T>A	ENSP00000485128.2:p.Met172Lys
ENST00000634537.1:c.32T>A	ENSP00000489208.1:p.Met11Lys
ENST00000635155.1:n.389T>A
NM_001282512.1:c.803T>A	NP_001269441.1:p.Met268Lys
NM_006440.4:c.803T>A	NP_006431.2:p.Met268Lys
NM_001282512.2:c.803T>A	NP_001269441.1:p.Met268Lys
NM_001352300.1:c.800T>A	NP_001339229.1:p.Met267Lys
NM_001352301.1:c.713T>A	NP_001339230.1:p.Met238Lys
NM_001352302.1:c.515T>A	NP_001339231.1:p.Met172Lys
NM_001352303.1:c.707T>A	NP_001339232.1:p.Met236Lys
NR_147957.1:n.935T>A
NM_006440.5:c.803T>A MANE Select	NP_006431.2:p.Met268Lys
NM_001282512.3:c.803T>A	NP_001269441.1:p.Met268Lys
NM_001352300.2:c.800T>A	NP_001339229.1:p.Met267Lys
NR_147957.2:n.761T>A
NM_001352301.2:c.713T>A	NP_001339230.1:p.Met238Lys
NM_001352302.2:c.515T>A	NP_001339231.1:p.Met172Lys
NM_001352303.2:c.707T>A	NP_001339232.1:p.Met236Lys