Canonical Allele Identifier: CA1664276998

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877009C= , CM000668.2:g.131877009C=	GRCh38
NC_000006.11:g.132198149C= , CM000668.1:g.132198149C=	GRCh37
NC_000006.10:g.132239842C=	NCBI36
NG_008206.1:g.73994C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683687.1:n.613C=
ENST00000684536.1:n.239C=
ENST00000647893.1:c.1741C= MANE Select	ENSP00000498074.1:p.Pro581=
ENST00000647981.1:n.426C=
ENST00000650437.1:c.1232C=
ENST00000360971.6:c.1741C=	ENSP00000354238.2:p.Pro581=
ENST00000459624.1:n.785C=
ENST00000513998.5:c.*578C=	ENSP00000422424.1:n.*578C=
NM_006208.2:c.1741C=	NP_006199.2:p.Pro581=
XM_011535896.1:c.631C=	XP_011534198.1:p.Pro211=
NM_006208.3:c.1741C= MANE Select	NP_006199.2:p.Pro581=