Canonical Allele Identifier: CA365651791

Gene: ENPP1

Linked Data

• MyVariant Identifiers: chr6:g.132198141A>T (hg19) ; chr6:g.131877001A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131877001A>T , CM000668.2:g.131877001A>T	GRCh38
NC_000006.11:g.132198141A>T , CM000668.1:g.132198141A>T	GRCh37
NC_000006.10:g.132239834A>T	NCBI36
NG_008206.1:g.73986A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683687.1:n.605A>T
ENST00000684536.1:n.231A>T
ENST00000647893.1:c.1733A>T MANE Select	ENSP00000498074.1:p.Asn578Ile
ENST00000647981.1:n.418A>T
ENST00000650437.1:c.1224A>T
ENST00000360971.6:c.1733A>T	ENSP00000354238.2:p.Asn578Ile
ENST00000459624.1:n.777A>T
ENST00000513998.5:c.*570A>T	ENSP00000422424.1:n.*570A>T
NM_006208.2:c.1733A>T	NP_006199.2:p.Asn578Ile
XM_011535896.1:c.623A>T	XP_011534198.1:p.Asn208Ile
NM_006208.3:c.1733A>T MANE Select	NP_006199.2:p.Asn578Ile