Canonical Allele Identifier: CA1664253650
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131850962C= , CM000668.2:g.131850962C= GRCh38
NC_000006.11:g.132172102C= , CM000668.1:g.132172102C= GRCh37
NC_000006.10:g.132213795C= NCBI36
NG_008206.1:g.47947C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.431-180C= MANE Select ENSP00000498074.1:n.431-180C=
ENST00000650147.1:c.109-180C=
ENST00000650437.1:c.108+856C=
ENST00000360971.6:c.431-180C= ENSP00000354238.2:n.431-180C=
ENST00000486853.1:n.451-180C=
ENST00000513998.5:c.431-180C= ENSP00000422424.1:n.431-180C=
NM_006208.2:c.431-180C= NP_006199.2:n.431-180C=
NM_006208.3:c.431-180C= MANE Select NP_006199.2:n.431-180C=