Canonical Allele Identifier: CA1664283222
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890622C= , CM000668.2:g.131890622C= GRCh38
NC_000006.11:g.132211762C= , CM000668.1:g.132211762C= GRCh37
NC_000006.10:g.132253455C= NCBI36
NG_008206.1:g.87607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1320C=
ENST00000647893.1:c.*111C= MANE Select ENSP00000498074.1:n.*111C=
ENST00000360971.6:c.*111C= ENSP00000354238.2:n.*111C=
ENST00000513998.5:c.*1726C= ENSP00000422424.1:n.*1726C=
NM_006208.2:c.*111C= NP_006199.2:n.*111C=
XM_011535896.1:c.*111C= XP_011534198.1:n.*111C=
NM_006208.3:c.*111C= MANE Select NP_006199.2:n.*111C=
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