Canonical Allele Identifier: CA1664228263

Gene: ENPP3

Linked Data

• dbSNP Id: rs528635171

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131737711C>A , CM000668.2:g.131737711C>A	GRCh38
NC_000006.11:g.132058851C>A , CM000668.1:g.132058851C>A	GRCh37
NC_000006.10:g.132100544C>A	NCBI36
NG_033982.1:g.105410C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357639.8:c.2167+279C>A MANE Select	ENSP00000350265.3:n.2167+279C>A
ENST00000357639.7:c.2167+279C>A	ENSP00000350265.3:n.2167+279C>A
ENST00000358229.6:c.*39+279C>A	ENSP00000350964.5:n.*39+279C>A
ENST00000414305.5:c.2167+279C>A	ENSP00000406261.1:n.2167+279C>A
NM_005021.3:c.2167+279C>A	NP_005012.2:n.2167+279C>A
NM_005021.4:c.2167+279C>A	NP_005012.2:n.2167+279C>A
NR_133007.1:n.2181+279C>A
XM_011535897.1:c.1405+279C>A	XP_011534199.1:n.1405+279C>A
XM_017010932.1:c.1936+279C>A	XP_016866421.1:n.1936+279C>A
XR_001743464.2:n.2365+279C>A
NM_005021.5:c.2167+279C>A MANE Select	NP_005012.2:n.2167+279C>A
NR_133007.2:n.2114+279C>A