Canonical Allele Identifier: CA1664253772

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131851267G= , CM000668.2:g.131851267G=	GRCh38
NC_000006.11:g.132172407G= , CM000668.1:g.132172407G=	GRCh37
NC_000006.10:g.132214100G=	NCBI36
NG_008206.1:g.48252G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647893.1:c.556G= MANE Select	ENSP00000498074.1:p.Gly186=
ENST00000650147.1:c.234G=
ENST00000650437.1:c.108+1161G=
ENST00000360971.6:c.556G=	ENSP00000354238.2:p.Gly186=
ENST00000486853.1:n.576G=
ENST00000513998.5:c.556G=	ENSP00000422424.1:p.Gly186=
NM_006208.2:c.556G=	NP_006199.2:p.Gly186=
NM_006208.3:c.556G= MANE Select	NP_006199.2:p.Gly186=