Canonical Allele Identifier: CA1664277071

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877165A= , CM000668.2:g.131877165A=	GRCh38
NC_000006.11:g.132198305A= , CM000668.1:g.132198305A=	GRCh37
NC_000006.10:g.132239998A=	NCBI36
NG_008206.1:g.74150A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683687.1:n.769A=
ENST00000684536.1:n.395A=
ENST00000647893.1:c.1893+4A= MANE Select	ENSP00000498074.1:n.1893+4A=
ENST00000647981.1:n.578+4A=
ENST00000650437.1:c.1388A=
ENST00000360971.6:c.1893+4A=	ENSP00000354238.2:n.1893+4A=
ENST00000459624.1:n.941A=
ENST00000513998.5:c.*730+4A=	ENSP00000422424.1:n.*730+4A=
NM_006208.2:c.1893+4A=	NP_006199.2:n.1893+4A=
XM_011535896.1:c.783+4A=	XP_011534198.1:n.783+4A=
NM_006208.3:c.1893+4A= MANE Select	NP_006199.2:n.1893+4A=