Canonical Allele Identifier: CA1664283215

Gene: ENPP1

Linked Data

• dbSNP Id: rs1782456261

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131890612A>G , CM000668.2:g.131890612A>G	GRCh38
NC_000006.11:g.132211752A>G , CM000668.1:g.132211752A>G	GRCh37
NC_000006.10:g.132253445A>G	NCBI36
NG_008206.1:g.87597A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684674.1:n.1310A>G
ENST00000647893.1:c.*101A>G MANE Select	ENSP00000498074.1:n.*101A>G
ENST00000360971.6:c.*101A>G	ENSP00000354238.2:n.*101A>G
ENST00000513998.5:c.*1716A>G	ENSP00000422424.1:n.*1716A>G
NM_006208.2:c.*101A>G	NP_006199.2:n.*101A>G
XM_011535896.1:c.*101A>G	XP_011534198.1:n.*101A>G
NM_006208.3:c.*101A>G MANE Select	NP_006199.2:n.*101A>G