Canonical Allele Identifier: CA1664277004

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877017T= , CM000668.2:g.131877017T=	GRCh38
NC_000006.11:g.132198157T= , CM000668.1:g.132198157T=	GRCh37
NC_000006.10:g.132239850T=	NCBI36
NG_008206.1:g.74002T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683687.1:n.621T=
ENST00000684536.1:n.247T=
ENST00000647893.1:c.1749T= MANE Select	ENSP00000498074.1:p.Pro583=
ENST00000647981.1:n.434T=
ENST00000650437.1:c.1240T=
ENST00000360971.6:c.1749T=	ENSP00000354238.2:p.Pro583=
ENST00000459624.1:n.793T=
ENST00000513998.5:c.*586T=	ENSP00000422424.1:n.*586T=
NM_006208.2:c.1749T=	NP_006199.2:p.Pro583=
XM_011535896.1:c.639T=	XP_011534198.1:p.Pro213=
NM_006208.3:c.1749T= MANE Select	NP_006199.2:p.Pro583=