Canonical Allele Identifier: CA1664228272

Gene: ENPP3

Linked Data

• dbSNP Id: rs954520726

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131737725A>G , CM000668.2:g.131737725A>G	GRCh38
NC_000006.11:g.132058865A>G , CM000668.1:g.132058865A>G	GRCh37
NC_000006.10:g.132100558A>G	NCBI36
NG_033982.1:g.105424A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357639.8:c.2167+293A>G MANE Select	ENSP00000350265.3:n.2167+293A>G
ENST00000357639.7:c.2167+293A>G	ENSP00000350265.3:n.2167+293A>G
ENST00000358229.6:c.*39+293A>G	ENSP00000350964.5:n.*39+293A>G
ENST00000414305.5:c.2167+293A>G	ENSP00000406261.1:n.2167+293A>G
NM_005021.3:c.2167+293A>G	NP_005012.2:n.2167+293A>G
NM_005021.4:c.2167+293A>G	NP_005012.2:n.2167+293A>G
NR_133007.1:n.2181+293A>G
XM_011535897.1:c.1405+293A>G	XP_011534199.1:n.1405+293A>G
XM_017010932.1:c.1936+293A>G	XP_016866421.1:n.1936+293A>G
XR_001743464.2:n.2365+293A>G
NM_005021.5:c.2167+293A>G MANE Select	NP_005012.2:n.2167+293A>G
NR_133007.2:n.2114+293A>G