Canonical Allele Identifier: CA1143355796

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093228_197093231delinsAATG , CM000663.2:g.197093228_197093231delinsAATG	GRCh38
NC_000001.10:g.197062358_197062361delinsAATG , CM000663.1:g.197062358_197062361delinsAATG	GRCh37
NC_000001.9:g.195328981_195328984delinsAATG	NCBI36
NG_015867.1:g.58464_58467delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2402_2405delinsCATT
ENST00000367409.9:c.9115_9118delinsCATT MANE Select	ENSP00000356379.4:p.His3039=
ENST00000680265.1:c.9337_9340delinsCATT	ENSP00000505384.1:p.His3113=
ENST00000680710.1:c.9115_9118delinsCATT	ENSP00000506676.1:p.His3039=
ENST00000294732.11:c.4360_4363delinsCATT	ENSP00000294732.7:p.His1454=
ENST00000367408.5:c.2110_2113delinsCATT	ENSP00000356378.1:p.His704=
ENST00000367409.8:c.9115_9118delinsCATT	ENSP00000356379.4:p.His3039=
ENST00000612785.1:c.3073_3076delinsCATT	ENSP00000479244.1:p.His1025=
NM_001206846.1:c.4360_4363delinsCATT	NP_001193775.1:p.His1454=
NM_018136.4:c.9115_9118delinsCATT	NP_060606.3:p.His3039=
NM_018136.5:c.9115_9118delinsCATT MANE Select	NP_060606.3:p.His3039=
NM_001206846.2:c.4360_4363delinsCATT	NP_001193775.1:p.His1454=