Canonical Allele Identifier: CA1664253774

Gene: ENPP1

Linked Data

• dbSNP Id: rs1408246785

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131851270C>G , CM000668.2:g.131851270C>G	GRCh38
NC_000006.11:g.132172410C>G , CM000668.1:g.132172410C>G	GRCh37
NC_000006.10:g.132214103C>G	NCBI36
NG_008206.1:g.48255C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647893.1:c.556+3C>G MANE Select	ENSP00000498074.1:n.556+3C>G
ENST00000650147.1:c.234+3C>G
ENST00000650437.1:c.108+1164C>G
ENST00000360971.6:c.556+3C>G	ENSP00000354238.2:n.556+3C>G
ENST00000486853.1:n.579C>G
ENST00000513998.5:c.556+3C>G	ENSP00000422424.1:n.556+3C>G
NM_006208.2:c.556+3C>G	NP_006199.2:n.556+3C>G
NM_006208.3:c.556+3C>G MANE Select	NP_006199.2:n.556+3C>G