Canonical Allele Identifier: CA147911994
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs774172740
MyVariant Identifiers: chr6:g.132153811T>A (hg19) chr6:g.131832671T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832671T>A , CM000668.2:g.131832671T>A GRCh38
NC_000006.11:g.132153811T>A , CM000668.1:g.132153811T>A GRCh37
NC_000006.10:g.132195504T>A NCBI36
NG_008206.1:g.29656T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.241-15105T>A MANE Select ENSP00000498074.1:n.241-15105T>A
ENST00000650507.1:c.247+6556T>A ENSP00000497375.1:n.247+6556T>A
ENST00000360971.6:c.241-15105T>A ENSP00000354238.2:n.241-15105T>A
ENST00000486853.1:n.261-15105T>A
ENST00000513998.5:c.241-15105T>A ENSP00000422424.1:n.241-15105T>A
NM_006208.2:c.241-15105T>A NP_006199.2:n.241-15105T>A
NM_006208.3:c.241-15105T>A MANE Select NP_006199.2:n.241-15105T>A
Search 100 bp 5'
Search 100 bp 3'