Canonical Allele Identifier: CA1664277028

Gene: ENPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877071G= , CM000668.2:g.131877071G=	GRCh38
NC_000006.11:g.132198211G= , CM000668.1:g.132198211G=	GRCh37
NC_000006.10:g.132239904G=	NCBI36
NG_008206.1:g.74056G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683687.1:n.675G=
ENST00000684536.1:n.301G=
ENST00000647893.1:c.1803G= MANE Select	ENSP00000498074.1:p.Thr601=
ENST00000647981.1:n.488G=
ENST00000650437.1:c.1294G=
ENST00000360971.6:c.1803G=	ENSP00000354238.2:p.Thr601=
ENST00000459624.1:n.847G=
ENST00000513998.5:c.*640G=	ENSP00000422424.1:n.*640G=
NM_006208.2:c.1803G=	NP_006199.2:p.Thr601=
XM_011535896.1:c.693G=	XP_011534198.1:p.Thr231=
NM_006208.3:c.1803G= MANE Select	NP_006199.2:p.Thr601=