Canonical Allele Identifier: CA365665859

Gene: ENPP1

Linked Data

• MyVariant Identifiers: chr6:g.132179806A>T (hg19) ; chr6:g.131858666A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131858666A>T , CM000668.2:g.131858666A>T	GRCh38
NC_000006.11:g.132179806A>T , CM000668.1:g.132179806A>T	GRCh37
NC_000006.10:g.132221499A>T	NCBI36
NG_008206.1:g.55651A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647893.1:c.716-2A>T MANE Select	ENSP00000498074.1:n.716-2A>T
ENST00000650147.1:c.333-2A>T
ENST00000650437.1:c.207-2A>T
ENST00000360971.6:c.716-2A>T	ENSP00000354238.2:n.716-2A>T
ENST00000513998.5:c.716-2A>T	ENSP00000422424.1:n.716-2A>T
NM_006208.2:c.716-2A>T	NP_006199.2:n.716-2A>T
NM_006208.3:c.716-2A>T MANE Select	NP_006199.2:n.716-2A>T