Canonical Allele Identifier: CA377822835
Community Standard Title: NM_001776.6(ENTPD1):c.536G>A (p.Trp179Ter)
Gene: ENTPD1 HGNC NCBI
ENTPD1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95844598G>A , CM000672.2:g.95844598G>A GRCh38
NC_000010.10:g.97604355G>A , CM000672.1:g.97604355G>A GRCh37
NC_000010.9:g.97594345G>A NCBI36
NG_042803.1:g.137820G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001776.6:c.536G>A (ENTPD1) MANE Select NP_001767.3:p.Trp179Ter
ENST00000371205.5:c.536G>A (ENTPD1) MANE Select ENSP00000360248.4:p.Trp179Ter
NM_001098175.1:c.557G>A (ENTPD1) NP_001091645.1:p.Trp186Ter
NM_001098175.2:c.557G>A (ENTPD1) NP_001091645.1:p.Trp186Ter
NM_001164178.1:c.572G>A (ENTPD1) NP_001157650.1:p.Trp191Ter
NM_001164179.1:c.536G>A (ENTPD1) NP_001157651.1:p.Trp179Ter
NM_001164179.2:c.536G>A (ENTPD1) NP_001157651.1:p.Trp179Ter
NM_001164181.1:c.212G>A (ENTPD1) NP_001157653.1:p.Trp71Ter
NM_001164182.1:c.122G>A (ENTPD1) NP_001157654.1:p.Trp41Ter
NM_001164182.2:c.122G>A (ENTPD1) NP_001157654.1:p.Trp41Ter
NM_001164183.1:c.122G>A (ENTPD1) NP_001157655.1:p.Trp41Ter
NM_001164183.2:c.122G>A (ENTPD1) NP_001157655.1:p.Trp41Ter
NM_001312654.1:c.212G>A (ENTPD1) NP_001299583.1:p.Trp71Ter
NM_001320916.1:c.572G>A (ENTPD1) NP_001307845.1:p.Trp191Ter
NM_001776.5:c.536G>A (ENTPD1) NP_001767.3:p.Trp179Ter
NR_038444.1:n.533+2794C>T (ENTPD1-AS1)
ENST00000371205.4:c.536G>A (ENTPD1) ENSP00000360248.4:p.Trp179Ter
ENST00000371206.6:n.521G>A (ENTPD1)
ENST00000371207.8:c.572G>A (ENTPD1) ENSP00000360250.3:p.Trp191Ter
ENST00000422161.2:n.24G>A (ENTPD1)
ENST00000453258.6:c.557G>A (ENTPD1) ENSP00000390955.2:p.Trp186Ter
ENST00000483213.6:c.133G>A (ENTPD1) ENSP00000489333.1:p.Gly45Arg
ENST00000490659.5:n.519G>A (ENTPD1)
ENST00000539125.6:c.122G>A ENSP00000440027.1:p.Trp41Ter
ENST00000543964.6:c.212G>A (ENTPD1) ENSP00000442968.1:p.Trp71Ter
ENST00000635076.1:c.*111G>A (ENTPD1) ENSP00000489250.1:n.*111G>A
ENST00000635677.1:n.389G>A (ENTPD1)
ENST00000639992.1:c.385G>A (ENTPD1) ENSP00000492183.1:p.Gly129Arg
XM_011540370.1:c.212G>A (ENTPD1) XP_011538672.1:p.Trp71Ter
XM_011540370.2:c.593G>A (ENTPD1) XP_011538672.2:p.Trp198Ter
XM_011540371.1:c.557G>A (ENTPD1) XP_011538673.1:p.Trp186Ter
XM_011540371.2:c.557G>A (ENTPD1) XP_011538673.1:p.Trp186Ter
XM_011540372.1:c.212G>A (ENTPD1) XP_011538674.1:p.Trp71Ter
XM_011540372.2:c.593G>A (ENTPD1) XP_011538674.2:p.Trp198Ter
XM_011540373.1:c.212G>A (ENTPD1) XP_011538675.1:p.Trp71Ter
XM_011540373.2:c.593G>A (ENTPD1) XP_011538675.2:p.Trp198Ter
XM_011540374.1:c.212G>A (ENTPD1) XP_011538676.1:p.Trp71Ter
XM_011540374.3:c.593G>A (ENTPD1) XP_011538676.2:p.Trp198Ter
XM_011540375.1:c.212G>A (ENTPD1) XP_011538677.1:p.Trp71Ter
XM_011540376.1:c.212G>A (ENTPD1) XP_011538678.1:p.Trp71Ter
XM_011540376.2:c.593G>A (ENTPD1) XP_011538678.2:p.Trp198Ter
XM_011540377.1:c.212G>A (ENTPD1) XP_011538679.1:p.Trp71Ter
XM_011540377.2:c.212G>A (ENTPD1) XP_011538679.1:p.Trp71Ter
XM_017016958.2:c.536G>A (ENTPD1) XP_016872447.1:p.Trp179Ter
XM_017016959.1:c.122G>A (ENTPD1) XP_016872448.1:p.Trp41Ter
XM_017016960.1:c.212G>A (ENTPD1) XP_016872449.1:p.Trp71Ter
XM_017016961.1:c.122G>A (ENTPD1) XP_016872450.1:p.Trp41Ter
XM_017016962.1:c.593G>A (ENTPD1) XP_016872451.1:p.Trp198Ter
XM_017016963.1:c.572G>A (ENTPD1) XP_016872452.1:p.Trp191Ter
XM_017016964.2:c.536G>A (ENTPD1) XP_016872453.1:p.Trp179Ter