Canonical Allele Identifier: CA5621247
Community Standard Title: NC_000010.11:g.95755766G>A
Gene: ENTPD1 HGNC NCBI
ENTPD1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95755766G>A , CM000672.2:g.95755766G>A GRCh38
NC_000010.10:g.97515523G>A , CM000672.1:g.97515523G>A GRCh37
NC_000010.9:g.97505513G>A NCBI36
NG_042803.1:g.48988G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001098175.1:c.37+43773G>A (ENTPD1) NP_001091645.1:n.37+43773G>A
NM_001098175.2:c.37+43773G>A (ENTPD1) NP_001091645.1:n.37+43773G>A
NM_001164178.1:c.52G>A (ENTPD1) NP_001157650.1:p.Glu18Lys
NM_001164181.1:c.-181G>A (ENTPD1) NP_001157653.1:n.-181G>A
NM_001312654.1:c.-355G>A (ENTPD1) NP_001299583.1:n.-355G>A
NM_001320916.1:c.52G>A (ENTPD1) NP_001307845.1:p.Glu18Lys
NR_038444.1:n.1702C>T (ENTPD1-AS1)
ENST00000371207.8:c.52G>A (ENTPD1) ENSP00000360250.3:p.Glu18Lys
ENST00000453258.6:c.37+43773G>A (ENTPD1) ENSP00000390955.2:n.37+43773G>A
ENST00000543964.6:c.-181G>A (ENTPD1) ENSP00000442968.1:n.-181G>A
ENST00000635677.1:n.20G>A (ENTPD1)
XM_011540371.1:c.37+43773G>A (ENTPD1) XP_011538673.1:n.37+43773G>A
XM_011540371.2:c.37+43773G>A (ENTPD1) XP_011538673.1:n.37+43773G>A
XM_011540377.1:c.-309+13559G>A (ENTPD1) XP_011538679.1:n.-309+13559G>A
XM_011540377.2:c.-309+13559G>A (ENTPD1) XP_011538679.1:n.-309+13559G>A
XM_017016960.1:c.-181G>A (ENTPD1) XP_016872449.1:n.-181G>A
XM_017016961.1:c.-248G>A (ENTPD1) XP_016872450.1:n.-248G>A
XM_017016963.1:c.52G>A (ENTPD1) XP_016872452.1:p.Glu18Lys