Canonical Allele Identifier: CA377824171

Gene: ENTPD1 ENTPD1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95860503T>A , CM000672.2:g.95860503T>A	GRCh38
NC_000010.10:g.97620260T>A , CM000672.1:g.97620260T>A	GRCh37
NC_000010.9:g.97610250T>A	NCBI36
NG_042803.1:g.153725T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001776.6:c.1109T>A (ENTPD1) MANE Select	NP_001767.3:p.Leu370Ter
ENST00000371205.5:c.1109T>A (ENTPD1) MANE Select	ENSP00000360248.4:p.Leu370Ter
NM_001098175.1:c.1130T>A (ENTPD1)	NP_001091645.1:p.Leu377Ter
NM_001098175.2:c.1130T>A (ENTPD1)	NP_001091645.1:p.Leu377Ter
NM_001164178.1:c.1145T>A (ENTPD1)	NP_001157650.1:p.Leu382Ter
NM_001164179.1:c.986T>A (ENTPD1)	NP_001157651.1:p.Leu329Ter
NM_001164179.2:c.986T>A (ENTPD1)	NP_001157651.1:p.Leu329Ter
NM_001164181.1:c.785T>A (ENTPD1)	NP_001157653.1:p.Leu262Ter
NM_001164182.1:c.695T>A (ENTPD1)	NP_001157654.1:p.Leu232Ter
NM_001164182.2:c.695T>A (ENTPD1)	NP_001157654.1:p.Leu232Ter
NM_001164183.1:c.695T>A (ENTPD1)	NP_001157655.1:p.Leu232Ter
NM_001164183.2:c.695T>A (ENTPD1)	NP_001157655.1:p.Leu232Ter
NM_001312654.1:c.785T>A (ENTPD1)	NP_001299583.1:p.Leu262Ter
NM_001320916.1:c.1145T>A (ENTPD1)	NP_001307845.1:p.Leu382Ter
NM_001776.5:c.1109T>A (ENTPD1)	NP_001767.3:p.Leu370Ter
NR_038444.1:n.440-13018A>T (ENTPD1-AS1)
ENST00000371205.4:c.1109T>A (ENTPD1)	ENSP00000360248.4:p.Leu370Ter
ENST00000371207.8:c.1145T>A (ENTPD1)	ENSP00000360250.3:p.Leu382Ter
ENST00000453258.6:c.1130T>A (ENTPD1)	ENSP00000390955.2:p.Leu377Ter
ENST00000539125.6:c.695T>A	ENSP00000440027.1:p.Leu232Ter
ENST00000543964.6:c.785T>A (ENTPD1)	ENSP00000442968.1:p.Leu262Ter
ENST00000635076.1:c.*684T>A (ENTPD1)	ENSP00000489250.1:n.*684T>A
ENST00000639992.1:c.*514T>A (ENTPD1)	ENSP00000492183.1:n.*514T>A
XM_011540370.1:c.785T>A (ENTPD1)	XP_011538672.1:p.Leu262Ter
XM_011540370.2:c.1166T>A (ENTPD1)	XP_011538672.2:p.Leu389Ter
XM_011540371.1:c.1130T>A (ENTPD1)	XP_011538673.1:p.Leu377Ter
XM_011540371.2:c.1130T>A (ENTPD1)	XP_011538673.1:p.Leu377Ter
XM_011540372.1:c.785T>A (ENTPD1)	XP_011538674.1:p.Leu262Ter
XM_011540372.2:c.1166T>A (ENTPD1)	XP_011538674.2:p.Leu389Ter
XM_011540373.1:c.785T>A (ENTPD1)	XP_011538675.1:p.Leu262Ter
XM_011540373.2:c.1166T>A (ENTPD1)	XP_011538675.2:p.Leu389Ter
XM_011540374.1:c.785T>A (ENTPD1)	XP_011538676.1:p.Leu262Ter
XM_011540374.3:c.1166T>A (ENTPD1)	XP_011538676.2:p.Leu389Ter
XM_011540375.1:c.785T>A (ENTPD1)	XP_011538677.1:p.Leu262Ter
XM_011540377.1:c.785T>A (ENTPD1)	XP_011538679.1:p.Leu262Ter
XM_011540377.2:c.785T>A (ENTPD1)	XP_011538679.1:p.Leu262Ter
XM_017016958.2:c.1109T>A (ENTPD1)	XP_016872447.1:p.Leu370Ter
XM_017016959.1:c.695T>A (ENTPD1)	XP_016872448.1:p.Leu232Ter
XM_017016960.1:c.785T>A (ENTPD1)	XP_016872449.1:p.Leu262Ter
XM_017016961.1:c.695T>A (ENTPD1)	XP_016872450.1:p.Leu232Ter