Canonical Allele Identifier: CA1664283035
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890222G= , CM000668.2:g.131890222G= GRCh38
NC_000006.11:g.132211362G= , CM000668.1:g.132211362G= GRCh37
NC_000006.10:g.132253055G= NCBI36
NG_008206.1:g.87207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1039-119G=
ENST00000647893.1:c.2608-119G= MANE Select ENSP00000498074.1:n.2608-119G=
ENST00000360971.6:c.2608-119G= ENSP00000354238.2:n.2608-119G=
ENST00000513998.5:c.*1445-119G= ENSP00000422424.1:n.*1445-119G=
NM_006208.2:c.2608-119G= NP_006199.2:n.2608-119G=
XM_011535896.1:c.1498-119G= XP_011534198.1:n.1498-119G=
NM_006208.3:c.2608-119G= MANE Select NP_006199.2:n.2608-119G=
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