Canonical Allele Identifier: CA452157191

Gene: ENPP1

Linked Data

• MyVariant Identifiers: chr6:g.132198298T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877158T>A , CM000668.2:g.131877158T>A	GRCh38
NC_000006.11:g.132198298T>A , CM000668.1:g.132198298T>A	GRCh37
NC_000006.10:g.132239991T>A	NCBI36
NG_008206.1:g.74143T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683687.1:n.762T>A
ENST00000684536.1:n.388T>A
ENST00000647893.1:c.1890T>A MANE Select	ENSP00000498074.1:p.Pro630=
ENST00000647981.1:n.575T>A
ENST00000650437.1:c.1381T>A
ENST00000360971.6:c.1890T>A	ENSP00000354238.2:p.Pro630=
ENST00000459624.1:n.934T>A
ENST00000513998.5:c.*727T>A	ENSP00000422424.1:n.*727T>A
NM_006208.2:c.1890T>A	NP_006199.2:p.Pro630=
XM_011535896.1:c.780T>A	XP_011534198.1:p.Pro260=
NM_006208.3:c.1890T>A MANE Select	NP_006199.2:p.Pro630=