Canonical Allele Identifier: CA1819739569

Gene: ASAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130317540_130317541delinsAG , CM000670.2:g.130317540_130317541delinsAG	GRCh38
NC_000008.10:g.131329786_131329787delinsAG , CM000670.1:g.131329786_131329787delinsAG	GRCh37
NC_000008.9:g.131398968_131398969delinsAG	NCBI36
NG_030354.1:g.131120_131121delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518721.6:c.186+40476_186+40477delinsCT MANE Select	ENSP00000429900.1:n.186+40476_186+40477delinsCT
ENST00000357668.2:c.165+40476_165+40477delinsCT	ENSP00000350297.2:n.165+40476_165+40477delinsCT
ENST00000518721.5:c.186+40476_186+40477delinsCT	ENSP00000429900.1:n.186+40476_186+40477delinsCT
ENST00000520927.5:c.*168+40476_*168+40477delinsCT	ENSP00000428629.1:n.*168+40476_*168+40477delinsCT
ENST00000521075.5:c.*168+40476_*168+40477delinsCT	ENSP00000428463.1:n.*168+40476_*168+40477delinsCT
ENST00000521426.5:c.165+40476_165+40477delinsCT	ENSP00000430917.1:n.165+40476_165+40477delinsCT
ENST00000524299.1:c.*168+40476_*168+40477delinsCT	ENSP00000429614.1:n.*168+40476_*168+40477delinsCT
ENST00000524367.5:n.96+23301_96+23302delinsCT
NM_001247996.1:c.165+40476_165+40477delinsCT	NP_001234925.1:n.165+40476_165+40477delinsCT
NM_018482.3:c.186+40476_186+40477delinsCT	NP_060952.2:n.186+40476_186+40477delinsCT
XM_005250925.1:c.186+40476_186+40477delinsCT	XP_005250982.1:n.186+40476_186+40477delinsCT
XM_006716563.2:c.186+40476_186+40477delinsCT	XP_006716626.1:n.186+40476_186+40477delinsCT
XM_006716564.1:c.165+40476_165+40477delinsCT	XP_006716627.1:n.165+40476_165+40477delinsCT
XM_006716565.2:c.-120-27403_-120-27402delinsCT	XP_006716628.1:n.-120-27403_-120-27402delinsCT
XM_006716566.1:c.186+40476_186+40477delinsCT	XP_006716629.1:n.186+40476_186+40477delinsCT
XM_006716567.2:c.10-80547_10-80546delinsCT	XP_006716630.1:n.10-80547_10-80546delinsCT
XM_011517052.1:c.186+40476_186+40477delinsCT	XP_011515354.1:n.186+40476_186+40477delinsCT
XM_011517053.1:c.165+40476_165+40477delinsCT	XP_011515355.1:n.165+40476_165+40477delinsCT
XR_928643.1:n.2769_2770delinsAG
XR_928644.1:n.2584_2585delinsAG
XR_928645.1:n.2612_2613delinsAG
NM_001362924.1:c.186+40476_186+40477delinsCT	NP_001349853.1:n.186+40476_186+40477delinsCT
NM_001362925.1:c.186+40476_186+40477delinsCT	NP_001349854.1:n.186+40476_186+40477delinsCT
NM_001362926.1:c.186+40476_186+40477delinsCT	NP_001349855.1:n.186+40476_186+40477delinsCT
XM_006716563.3:c.186+40476_186+40477delinsCT	XP_006716626.1:n.186+40476_186+40477delinsCT
XM_006716565.3:c.-120-27403_-120-27402delinsCT	XP_006716628.1:n.-120-27403_-120-27402delinsCT
XM_011517052.2:c.186+40476_186+40477delinsCT	XP_011515354.1:n.186+40476_186+40477delinsCT
XM_017013467.2:c.51+40141_51+40142delinsCT	XP_016868956.1:n.51+40141_51+40142delinsCT
XM_017013468.1:c.10-80547_10-80546delinsCT	XP_016868957.1:n.10-80547_10-80546delinsCT
NM_018482.4:c.186+40476_186+40477delinsCT MANE Select	NP_060952.2:n.186+40476_186+40477delinsCT
NM_001362925.2:c.186+40476_186+40477delinsCT	NP_001349854.1:n.186+40476_186+40477delinsCT
NM_001362926.2:c.186+40476_186+40477delinsCT	NP_001349855.1:n.186+40476_186+40477delinsCT
NM_001247996.2:c.165+40476_165+40477delinsCT	NP_001234925.1:n.165+40476_165+40477delinsCT