Canonical Allele Identifier: CA1664283089
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890331A= , CM000668.2:g.131890331A= GRCh38
NC_000006.11:g.132211471A= , CM000668.1:g.132211471A= GRCh37
NC_000006.10:g.132253164A= NCBI36
NG_008206.1:g.87316A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684674.1:n.1039-10A=
ENST00000647893.1:c.2608-10A= MANE Select ENSP00000498074.1:n.2608-10A=
ENST00000360971.6:c.2608-10A= ENSP00000354238.2:n.2608-10A=
ENST00000513998.5:c.*1445-10A= ENSP00000422424.1:n.*1445-10A=
NM_006208.2:c.2608-10A= NP_006199.2:n.2608-10A=
XM_011535896.1:c.1498-10A= XP_011534198.1:n.1498-10A=
NM_006208.3:c.2608-10A= MANE Select NP_006199.2:n.2608-10A=