Canonical Allele Identifier: CA13165487

Gene: ENTPD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95751280A>G , CM000672.2:g.95751280A>G	GRCh38
NC_000010.10:g.97511037A>G , CM000672.1:g.97511037A>G	GRCh37
NC_000010.9:g.97501027A>G	NCBI36
NG_042803.1:g.44502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453258.6:c.37+39287A>G	ENSP00000390955.2:n.37+39287A>G
NM_001098175.1:c.37+39287A>G	NP_001091645.1:n.37+39287A>G
XM_011540371.1:c.37+39287A>G	XP_011538673.1:n.37+39287A>G
XM_011540377.1:c.-309+9073A>G	XP_011538679.1:n.-309+9073A>G
XM_011540371.2:c.37+39287A>G	XP_011538673.1:n.37+39287A>G
XM_011540377.2:c.-309+9073A>G	XP_011538679.1:n.-309+9073A>G
NM_001098175.2:c.37+39287A>G	NP_001091645.1:n.37+39287A>G