Canonical Allele Identifier: CA1664283138

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131890432T= , CM000668.2:g.131890432T=	GRCh38
NC_000006.11:g.132211572T= , CM000668.1:g.132211572T=	GRCh37
NC_000006.10:g.132253265T=	NCBI36
NG_008206.1:g.87417T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684674.1:n.1130T=
ENST00000647893.1:c.2699T= MANE Select	ENSP00000498074.1:p.Phe900=
ENST00000360971.6:c.2699T=	ENSP00000354238.2:p.Phe900=
ENST00000513998.5:c.*1536T=	ENSP00000422424.1:n.*1536T=
NM_006208.2:c.2699T=	NP_006199.2:p.Phe900=
XM_011535896.1:c.1589T=	XP_011534198.1:p.Phe530=
NM_006208.3:c.2699T= MANE Select	NP_006199.2:p.Phe900=