Canonical Allele Identifier: CA1664237958
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131829304T= , CM000668.2:g.131829304T= GRCh38
NC_000006.11:g.132150444T= , CM000668.1:g.132150444T= GRCh37
NC_000006.10:g.132192137T= NCBI36
NG_008206.1:g.26289T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.241-18472T= MANE Select ENSP00000498074.1:n.241-18472T=
ENST00000650507.1:c.247+3189T= ENSP00000497375.1:n.247+3189T=
ENST00000360971.6:c.241-18472T= ENSP00000354238.2:n.241-18472T=
ENST00000486853.1:n.261-18472T=
ENST00000513998.5:c.241-18472T= ENSP00000422424.1:n.241-18472T=
NM_006208.2:c.241-18472T= NP_006199.2:n.241-18472T=
NM_006208.3:c.241-18472T= MANE Select NP_006199.2:n.241-18472T=