Canonical Allele Identifier: CA1664228260

Gene: ENPP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131737709C= , CM000668.2:g.131737709C=	GRCh38
NC_000006.11:g.132058849C= , CM000668.1:g.132058849C=	GRCh37
NC_000006.10:g.132100542C=	NCBI36
NG_033982.1:g.105408C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357639.8:c.2167+277C= MANE Select	ENSP00000350265.3:n.2167+277C=
ENST00000357639.7:c.2167+277C=	ENSP00000350265.3:n.2167+277C=
ENST00000358229.6:c.*39+277C=	ENSP00000350964.5:n.*39+277C=
ENST00000414305.5:c.2167+277C=	ENSP00000406261.1:n.2167+277C=
NM_005021.3:c.2167+277C=	NP_005012.2:n.2167+277C=
NM_005021.4:c.2167+277C=	NP_005012.2:n.2167+277C=
NR_133007.1:n.2181+277C=
XM_011535897.1:c.1405+277C=	XP_011534199.1:n.1405+277C=
XM_017010932.1:c.1936+277C=	XP_016866421.1:n.1936+277C=
XR_001743464.2:n.2365+277C=
NM_005021.5:c.2167+277C= MANE Select	NP_005012.2:n.2167+277C=
NR_133007.2:n.2114+277C=