Canonical Allele Identifier: CA1664283177
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1782455315
gnomAD v4: 6-131890521-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890522dup , CM000668.2:g.131890522dup GRCh38
NC_000006.11:g.132211662dup , CM000668.1:g.132211662dup GRCh37
NC_000006.10:g.132253355dup NCBI36
NG_008206.1:g.87507dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1220dup
ENST00000647893.1:c.*11dup MANE Select ENSP00000498074.1:n.*11dup
ENST00000360971.6:c.*11dup ENSP00000354238.2:n.*11dup
ENST00000513998.5:c.*1626dup ENSP00000422424.1:n.*1626dup
NM_006208.2:c.*11dup NP_006199.2:n.*11dup
XM_011535896.1:c.*11dup XP_011534198.1:n.*11dup
NM_006208.3:c.*11dup MANE Select NP_006199.2:n.*11dup
Search 100 bp 5'
Search 100 bp 3'