Canonical Allele Identifier: CA1819739708

Gene: ASAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130317853G= , CM000670.2:g.130317853G=	GRCh38
NC_000008.10:g.131330099G= , CM000670.1:g.131330099G=	GRCh37
NC_000008.9:g.131399281G=	NCBI36
NG_030354.1:g.130808C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518721.6:c.186+40164C= MANE Select	ENSP00000429900.1:n.186+40164C=
ENST00000357668.2:c.165+40164C=	ENSP00000350297.2:n.165+40164C=
ENST00000518721.5:c.186+40164C=	ENSP00000429900.1:n.186+40164C=
ENST00000520927.5:c.*168+40164C=	ENSP00000428629.1:n.*168+40164C=
ENST00000521075.5:c.*168+40164C=	ENSP00000428463.1:n.*168+40164C=
ENST00000521426.5:c.165+40164C=	ENSP00000430917.1:n.165+40164C=
ENST00000524299.1:c.*168+40164C=	ENSP00000429614.1:n.*168+40164C=
ENST00000524367.5:n.96+22989C=
NM_001247996.1:c.165+40164C=	NP_001234925.1:n.165+40164C=
NM_018482.3:c.186+40164C=	NP_060952.2:n.186+40164C=
XM_005250925.1:c.186+40164C=	XP_005250982.1:n.186+40164C=
XM_006716563.2:c.186+40164C=	XP_006716626.1:n.186+40164C=
XM_006716564.1:c.165+40164C=	XP_006716627.1:n.165+40164C=
XM_006716565.2:c.-120-27715C=	XP_006716628.1:n.-120-27715C=
XM_006716566.1:c.186+40164C=	XP_006716629.1:n.186+40164C=
XM_006716567.2:c.10-80859C=	XP_006716630.1:n.10-80859C=
XM_011517052.1:c.186+40164C=	XP_011515354.1:n.186+40164C=
XM_011517053.1:c.165+40164C=	XP_011515355.1:n.165+40164C=
XR_928643.1:n.3082G=
XR_928644.1:n.2897G=
XR_928645.1:n.2925G=
NM_001362924.1:c.186+40164C=	NP_001349853.1:n.186+40164C=
NM_001362925.1:c.186+40164C=	NP_001349854.1:n.186+40164C=
NM_001362926.1:c.186+40164C=	NP_001349855.1:n.186+40164C=
XM_006716563.3:c.186+40164C=	XP_006716626.1:n.186+40164C=
XM_006716565.3:c.-120-27715C=	XP_006716628.1:n.-120-27715C=
XM_011517052.2:c.186+40164C=	XP_011515354.1:n.186+40164C=
XM_017013467.2:c.51+39829C=	XP_016868956.1:n.51+39829C=
XM_017013468.1:c.10-80859C=	XP_016868957.1:n.10-80859C=
NM_018482.4:c.186+40164C= MANE Select	NP_060952.2:n.186+40164C=
NM_001362925.2:c.186+40164C=	NP_001349854.1:n.186+40164C=
NM_001362926.2:c.186+40164C=	NP_001349855.1:n.186+40164C=
NM_001247996.2:c.165+40164C=	NP_001234925.1:n.165+40164C=