Canonical Allele Identifier: CA513369065

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906436G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918913G>T , CM000684.2:g.19918913G>T	GRCh38
NC_000022.10:g.19906436G>T , CM000684.1:g.19906436G>T	GRCh37
NC_000022.9:g.18286436G>T	NCBI36
NG_011835.1:g.27924C>A , LRG_417:g.27924C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.321C>A MANE Select	ENSP00000383365.1:p.Ile107=
ENST00000334363.14:c.321C>A	ENSP00000334451.9:p.Ile107=
ENST00000400518.5:c.231C>A	ENSP00000383362.1:p.Ile77=
ENST00000400519.6:c.318C>A	ENSP00000383363.1:p.Ile106=
ENST00000400521.6:c.321C>A	ENSP00000383365.1:p.Ile107=
ENST00000400525.6:c.252C>A	ENSP00000383369.3:p.Ile84=
ENST00000474308.5:c.264C>A	ENSP00000485665.1:p.Ile88=
ENST00000491939.6:c.225C>A	ENSP00000485543.1:p.Ile75=
ENST00000496729.2:n.326C>A
ENST00000542719.6:c.33C>A	ENSP00000485128.2:p.Ile11=
NM_001282512.1:c.321C>A	NP_001269441.1:p.Ile107=
NM_006440.4:c.321C>A	NP_006431.2:p.Ile107=
NM_001282512.2:c.321C>A	NP_001269441.1:p.Ile107=
NM_001352300.1:c.318C>A	NP_001339229.1:p.Ile106=
NM_001352301.1:c.231C>A	NP_001339230.1:p.Ile77=
NM_001352302.1:c.33C>A	NP_001339231.1:p.Ile11=
NM_001352303.1:c.225C>A	NP_001339232.1:p.Ile75=
NR_147957.1:n.453C>A
NM_006440.5:c.321C>A MANE Select	NP_006431.2:p.Ile107=
NM_001282512.3:c.321C>A	NP_001269441.1:p.Ile107=
NM_001352300.2:c.318C>A	NP_001339229.1:p.Ile106=
NR_147957.2:n.279C>A
NM_001352301.2:c.231C>A	NP_001339230.1:p.Ile77=
NM_001352302.2:c.33C>A	NP_001339231.1:p.Ile11=
NM_001352303.2:c.225C>A	NP_001339232.1:p.Ile75=