Canonical Allele Identifier: CA365651921

Gene: ENPP1

Linked Data

• dbSNP Id: rs1468763329
• MyVariant Identifiers: chr6:g.132198155C>G (hg19) ; chr6:g.131877015C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877015C>G , CM000668.2:g.131877015C>G	GRCh38
NC_000006.11:g.132198155C>G , CM000668.1:g.132198155C>G	GRCh37
NC_000006.10:g.132239848C>G	NCBI36
NG_008206.1:g.74000C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683687.1:n.619C>G
ENST00000684536.1:n.245C>G
ENST00000647893.1:c.1747C>G MANE Select	ENSP00000498074.1:p.Pro583Ala
ENST00000647981.1:n.432C>G
ENST00000650437.1:c.1238C>G
ENST00000360971.6:c.1747C>G	ENSP00000354238.2:p.Pro583Ala
ENST00000459624.1:n.791C>G
ENST00000513998.5:c.*584C>G	ENSP00000422424.1:n.*584C>G
NM_006208.2:c.1747C>G	NP_006199.2:p.Pro583Ala
XM_011535896.1:c.637C>G	XP_011534198.1:p.Pro213Ala
NM_006208.3:c.1747C>G MANE Select	NP_006199.2:p.Pro583Ala