Canonical Allele Identifier: CA2578742756
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851106A>T , CM000668.2:g.131851106A>T GRCh38
NC_000006.11:g.132172246A>T , CM000668.1:g.132172246A>T GRCh37
NC_000006.10:g.132213939A>T NCBI36
NG_008206.1:g.48091A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.431-36A>T MANE Select ENSP00000498074.1:n.431-36A>T
ENST00000650147.1:c.109-36A>T
ENST00000650437.1:c.108+1000A>T
ENST00000360971.6:c.431-36A>T ENSP00000354238.2:n.431-36A>T
ENST00000486853.1:n.451-36A>T
ENST00000513998.5:c.431-36A>T ENSP00000422424.1:n.431-36A>T
NM_006208.2:c.431-36A>T NP_006199.2:n.431-36A>T
NM_006208.3:c.431-36A>T MANE Select NP_006199.2:n.431-36A>T