Canonical Allele Identifier: CA1139849874

Gene: ASAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23439740C= , CM000663.2:g.23439740C=	GRCh38
NC_000001.10:g.23766233C= , CM000663.1:g.23766233C=	GRCh37
NC_000001.9:g.23638820C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017707.4:c.945-510G= MANE Select	NP_060177.2:n.945-510G=
ENST00000336689.8:c.945-510G= MANE Select	ENSP00000338769.3:n.945-510G=
NM_001143778.1:c.918-510G=	NP_001137250.1:n.918-510G=
NM_001143778.2:c.918-510G=	NP_001137250.1:n.918-510G=
NM_017707.3:c.945-510G=	NP_060177.2:n.945-510G=
ENST00000336689.7:c.945-510G=	ENSP00000338769.3:n.945-510G=
ENST00000437606.6:c.918-510G=	ENSP00000408826.2:n.918-510G=
ENST00000475814.5:c.360-906G=	ENSP00000436439.1:n.360-906G=
ENST00000492982.6:c.*779-510G=	ENSP00000435858.1:n.*779-510G=
ENST00000618240.4:c.527+2819G=	ENSP00000483740.1:n.527+2819G=
ENST00000711425.1:c.*596-510G=	ENSP00000518742.1:n.*596-510G=
ENST00000711426.1:c.1066-510G=	ENSP00000518743.1:n.1066-510G=
ENST00000711427.1:c.552-510G=	ENSP00000518744.1:n.552-510G=
XM_011541754.1:c.1002-510G=	XP_011540056.1:n.1002-510G=
XM_011541755.1:c.951-510G=	XP_011540057.1:n.951-510G=
XM_011541755.2:c.951-510G=	XP_011540057.1:n.951-510G=
XM_011541756.1:c.1008-510G=	XP_011540058.1:n.1008-510G=
XM_011541757.1:c.1002-510G=	XP_011540059.1:n.1002-510G=
XM_011541758.1:c.873-510G=	XP_011540060.1:n.873-510G=
XM_017001685.2:c.945-510G=	XP_016857174.1:n.945-510G=
XM_017001686.2:c.951-510G=	XP_016857175.1:n.951-510G=
XM_017001687.1:c.885-510G=	XP_016857176.1:n.885-510G=
XM_017001688.2:c.552-510G=	XP_016857177.1:n.552-510G=
XM_017001689.1:c.558-510G=	XP_016857178.1:n.558-510G=