Canonical Allele Identifier: CA410686620

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883017G>C (hg19) ; chr22:g.19895494G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895494G>C , CM000684.2:g.19895494G>C	GRCh38
NC_000022.10:g.19883017G>C , CM000684.1:g.19883017G>C	GRCh37
NC_000022.9:g.18263017G>C	NCBI36
NG_011835.1:g.51343C>G , LRG_417:g.51343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.862C>G MANE Select	ENSP00000383365.1:p.Pro288Ala
ENST00000334363.14:c.862C>G	ENSP00000334451.9:p.Pro288Ala
ENST00000400518.5:c.772C>G	ENSP00000383362.1:p.Pro258Ala
ENST00000400519.6:c.859C>G	ENSP00000383363.1:p.Pro287Ala
ENST00000400521.6:c.862C>G	ENSP00000383365.1:p.Pro288Ala
ENST00000400525.6:c.793C>G	ENSP00000383369.3:p.Pro265Ala
ENST00000474308.5:c.805C>G	ENSP00000485665.1:p.Pro269Ala
ENST00000475995.3:c.359C>G
ENST00000491939.6:c.766C>G	ENSP00000485543.1:p.Pro256Ala
ENST00000494454.5:n.936C>G
ENST00000542719.6:c.574C>G	ENSP00000485128.2:p.Pro192Ala
ENST00000634537.1:c.91C>G	ENSP00000489208.1:p.Pro31Ala
ENST00000635155.1:n.448C>G
NM_001282512.1:c.862C>G	NP_001269441.1:p.Pro288Ala
NM_006440.4:c.862C>G	NP_006431.2:p.Pro288Ala
NM_001282512.2:c.862C>G	NP_001269441.1:p.Pro288Ala
NM_001352300.1:c.859C>G	NP_001339229.1:p.Pro287Ala
NM_001352301.1:c.772C>G	NP_001339230.1:p.Pro258Ala
NM_001352302.1:c.574C>G	NP_001339231.1:p.Pro192Ala
NM_001352303.1:c.766C>G	NP_001339232.1:p.Pro256Ala
NR_147957.1:n.994C>G
NM_006440.5:c.862C>G MANE Select	NP_006431.2:p.Pro288Ala
NM_001282512.3:c.862C>G	NP_001269441.1:p.Pro288Ala
NM_001352300.2:c.859C>G	NP_001339229.1:p.Pro287Ala
NR_147957.2:n.820C>G
NM_001352301.2:c.772C>G	NP_001339230.1:p.Pro258Ala
NM_001352302.2:c.574C>G	NP_001339231.1:p.Pro192Ala
NM_001352303.2:c.766C>G	NP_001339232.1:p.Pro256Ala