Canonical Allele Identifier: CA1664228267

Gene: ENPP3

Linked Data

• dbSNP Id: rs1780429297

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131737715A>G , CM000668.2:g.131737715A>G	GRCh38
NC_000006.11:g.132058855A>G , CM000668.1:g.132058855A>G	GRCh37
NC_000006.10:g.132100548A>G	NCBI36
NG_033982.1:g.105414A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357639.8:c.2167+283A>G MANE Select	ENSP00000350265.3:n.2167+283A>G
ENST00000357639.7:c.2167+283A>G	ENSP00000350265.3:n.2167+283A>G
ENST00000358229.6:c.*39+283A>G	ENSP00000350964.5:n.*39+283A>G
ENST00000414305.5:c.2167+283A>G	ENSP00000406261.1:n.2167+283A>G
NM_005021.3:c.2167+283A>G	NP_005012.2:n.2167+283A>G
NM_005021.4:c.2167+283A>G	NP_005012.2:n.2167+283A>G
NR_133007.1:n.2181+283A>G
XM_011535897.1:c.1405+283A>G	XP_011534199.1:n.1405+283A>G
XM_017010932.1:c.1936+283A>G	XP_016866421.1:n.1936+283A>G
XR_001743464.2:n.2365+283A>G
NM_005021.5:c.2167+283A>G MANE Select	NP_005012.2:n.2167+283A>G
NR_133007.2:n.2114+283A>G