Canonical Allele Identifier: CA1664283152

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131890480C= , CM000668.2:g.131890480C=	GRCh38
NC_000006.11:g.132211620C= , CM000668.1:g.132211620C=	GRCh37
NC_000006.10:g.132253313C=	NCBI36
NG_008206.1:g.87465C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684674.1:n.1178C=
ENST00000647893.1:c.2747C= MANE Select	ENSP00000498074.1:p.Thr916=
ENST00000360971.6:c.2747C=	ENSP00000354238.2:p.Thr916=
ENST00000513998.5:c.*1584C=	ENSP00000422424.1:n.*1584C=
NM_006208.2:c.2747C=	NP_006199.2:p.Thr916=
XM_011535896.1:c.1637C=	XP_011534198.1:p.Thr546=
NM_006208.3:c.2747C= MANE Select	NP_006199.2:p.Thr916=