Canonical Allele Identifier: CA1819627987

Gene: ASAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130080083A= , CM000670.2:g.130080083A=	GRCh38
NC_000008.10:g.131092329A= , CM000670.1:g.131092329A=	GRCh37
NC_000008.9:g.131161511A=	NCBI36
NG_030354.1:g.368578T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000518721.6:c.2573-112T= MANE Select	ENSP00000429900.1:n.2573-112T=
ENST00000357668.2:c.2552-112T=	ENSP00000350297.2:n.2552-112T=
ENST00000518721.5:c.2573-112T=	ENSP00000429900.1:n.2573-112T=
ENST00000519483.5:c.642-112T=
ENST00000520189.1:n.493-112T=
ENST00000521075.5:c.*2555-112T=	ENSP00000428463.1:n.*2555-112T=
ENST00000524124.5:c.2034-112T=
NM_001247996.1:c.2552-112T=	NP_001234925.1:n.2552-112T=
NM_018482.3:c.2573-112T=	NP_060952.2:n.2573-112T=
XM_005250925.1:c.2582-112T=	XP_005250982.1:n.2582-112T=
XM_006716563.2:c.2582-112T=	XP_006716626.1:n.2582-112T=
XM_006716564.1:c.2561-112T=	XP_006716627.1:n.2561-112T=
XM_006716565.2:c.2414-112T=	XP_006716628.1:n.2414-112T=
XM_006716566.1:c.2411-112T=	XP_006716629.1:n.2411-112T=
XM_006716567.2:c.2405-112T=	XP_006716630.1:n.2405-112T=
XM_011517052.1:c.2582-112T=	XP_011515354.1:n.2582-112T=
XM_011517053.1:c.2561-112T=	XP_011515355.1:n.2561-112T=
NM_001362924.1:c.2582-112T=	NP_001349853.1:n.2582-112T=
NM_001362925.1:c.2411-112T=	NP_001349854.1:n.2411-112T=
NM_001362926.1:c.2402-112T=	NP_001349855.1:n.2402-112T=
XM_006716563.3:c.2582-112T=	XP_006716626.1:n.2582-112T=
XM_006716565.3:c.2414-112T=	XP_006716628.1:n.2414-112T=
XM_011517052.2:c.2582-112T=	XP_011515354.1:n.2582-112T=
XM_017013467.2:c.2447-112T=	XP_016868956.1:n.2447-112T=
XM_017013468.1:c.2405-112T=	XP_016868957.1:n.2405-112T=
NM_018482.4:c.2573-112T= MANE Select	NP_060952.2:n.2573-112T=
NM_001362925.2:c.2411-112T=	NP_001349854.1:n.2411-112T=
NM_001362926.2:c.2402-112T=	NP_001349855.1:n.2402-112T=
NM_001247996.2:c.2552-112T=	NP_001234925.1:n.2552-112T=