Canonical Allele Identifier: CA16042268
Gene: TAX1BP3 HGNC NCBI
P2RX5-TAX1BP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 372264
ClinVar RCV Id: RCV000412628
dbSNP Id: rs1057517690
MyVariant Identifiers: chr17:g.3568034A>G (hg19) chr17:g.3664740A>G (hg38)
PubMed: PMID:25645515
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3664740A>G , CM000679.2:g.3664740A>G GRCh38
NC_000017.10:g.3568034A>G , CM000679.1:g.3568034A>G GRCh37
NC_000017.9:g.3514783A>G NCBI36
NG_012489.1:g.33273A>G
NG_053154.1:g.8940T>C
NG_012489.2:g.33273A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225525.4:c.98T>C (TAX1BP3) MANE Select ENSP00000225525.3:p.Ile33Thr
ENST00000225525.3:c.98T>C (TAX1BP3) ENSP00000225525.3:p.Ile33Thr
ENST00000550383.1:c.*3455T>C (P2RX5-TAX1BP3) ENSP00000455681.1:n.*3455T>C
ENST00000611779.4:c.98T>C (TAX1BP3) ENSP00000484776.1:p.Ile33Thr
NM_001204698.1:c.98T>C (TAX1BP3) NP_001191627.1:p.Ile33Thr
NM_014604.3:c.98T>C (TAX1BP3) NP_055419.1:p.Ile33Thr
NR_037928.1:n.5153T>C (P2RX5-TAX1BP3)
NM_014604.4:c.98T>C (TAX1BP3) MANE Select NP_055419.1:p.Ile33Thr
NM_001204698.2:c.98T>C (TAX1BP3) NP_001191627.1:p.Ile33Thr
Search 100 bp 5'
Search 100 bp 3'