Canonical Allele Identifier: CA2500502870

Gene: ASAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130317808_130317809insCATT , CM000670.2:g.130317808_130317809insCATT	GRCh38
NC_000008.10:g.131330054_131330055insCATT , CM000670.1:g.131330054_131330055insCATT	GRCh37
NC_000008.9:g.131399236_131399237insCATT	NCBI36
NG_030354.1:g.130853_130854insATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518721.6:c.186+40209_186+40210insATGA MANE Select	ENSP00000429900.1:n.186+40209_186+40210insATGA
ENST00000357668.2:c.165+40209_165+40210insATGA	ENSP00000350297.2:n.165+40209_165+40210insATGA
ENST00000518721.5:c.186+40209_186+40210insATGA	ENSP00000429900.1:n.186+40209_186+40210insATGA
ENST00000520927.5:c.*168+40209_*168+40210insATGA	ENSP00000428629.1:n.*168+40209_*168+40210insATGA
ENST00000521075.5:c.*168+40209_*168+40210insATGA	ENSP00000428463.1:n.*168+40209_*168+40210insATGA
ENST00000521426.5:c.165+40209_165+40210insATGA	ENSP00000430917.1:n.165+40209_165+40210insATGA
ENST00000524299.1:c.*168+40209_*168+40210insATGA	ENSP00000429614.1:n.*168+40209_*168+40210insATGA
ENST00000524367.5:n.96+23034_96+23035insATGA
NM_001247996.1:c.165+40209_165+40210insATGA	NP_001234925.1:n.165+40209_165+40210insATGA
NM_018482.3:c.186+40209_186+40210insATGA	NP_060952.2:n.186+40209_186+40210insATGA
XM_005250925.1:c.186+40209_186+40210insATGA	XP_005250982.1:n.186+40209_186+40210insATGA
XM_006716563.2:c.186+40209_186+40210insATGA	XP_006716626.1:n.186+40209_186+40210insATGA
XM_006716564.1:c.165+40209_165+40210insATGA	XP_006716627.1:n.165+40209_165+40210insATGA
XM_006716565.2:c.-120-27670_-120-27669insATGA	XP_006716628.1:n.-120-27670_-120-27669insATGA
XM_006716566.1:c.186+40209_186+40210insATGA	XP_006716629.1:n.186+40209_186+40210insATGA
XM_006716567.2:c.10-80814_10-80813insATGA	XP_006716630.1:n.10-80814_10-80813insATGA
XM_011517052.1:c.186+40209_186+40210insATGA	XP_011515354.1:n.186+40209_186+40210insATGA
XM_011517053.1:c.165+40209_165+40210insATGA	XP_011515355.1:n.165+40209_165+40210insATGA
XR_928643.1:n.3037_3038insCATT
XR_928644.1:n.2852_2853insCATT
XR_928645.1:n.2880_2881insCATT
NM_001362924.1:c.186+40209_186+40210insATGA	NP_001349853.1:n.186+40209_186+40210insATGA
NM_001362925.1:c.186+40209_186+40210insATGA	NP_001349854.1:n.186+40209_186+40210insATGA
NM_001362926.1:c.186+40209_186+40210insATGA	NP_001349855.1:n.186+40209_186+40210insATGA
XM_006716563.3:c.186+40209_186+40210insATGA	XP_006716626.1:n.186+40209_186+40210insATGA
XM_006716565.3:c.-120-27670_-120-27669insATGA	XP_006716628.1:n.-120-27670_-120-27669insATGA
XM_011517052.2:c.186+40209_186+40210insATGA	XP_011515354.1:n.186+40209_186+40210insATGA
XM_017013467.2:c.51+39874_51+39875insATGA	XP_016868956.1:n.51+39874_51+39875insATGA
XM_017013468.1:c.10-80814_10-80813insATGA	XP_016868957.1:n.10-80814_10-80813insATGA
NM_018482.4:c.186+40209_186+40210insATGA MANE Select	NP_060952.2:n.186+40209_186+40210insATGA
NM_001362925.2:c.186+40209_186+40210insATGA	NP_001349854.1:n.186+40209_186+40210insATGA
NM_001362926.2:c.186+40209_186+40210insATGA	NP_001349855.1:n.186+40209_186+40210insATGA
NM_001247996.2:c.165+40209_165+40210insATGA	NP_001234925.1:n.165+40209_165+40210insATGA