Canonical Allele Identifier: CA1664283201
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1782455952

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890557T>A , CM000668.2:g.131890557T>A GRCh38
NC_000006.11:g.132211697T>A , CM000668.1:g.132211697T>A GRCh37
NC_000006.10:g.132253390T>A NCBI36
NG_008206.1:g.87542T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1255T>A
ENST00000647893.1:c.*46T>A MANE Select ENSP00000498074.1:n.*46T>A
ENST00000360971.6:c.*46T>A ENSP00000354238.2:n.*46T>A
ENST00000513998.5:c.*1661T>A ENSP00000422424.1:n.*1661T>A
NM_006208.2:c.*46T>A NP_006199.2:n.*46T>A
XM_011535896.1:c.*46T>A XP_011534198.1:n.*46T>A
NM_006208.3:c.*46T>A MANE Select NP_006199.2:n.*46T>A