Canonical Allele Identifier: CA1217930470

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102912_197102914delinsAAT , CM000663.2:g.197102912_197102914delinsAAT	GRCh38
NC_000001.10:g.197072042_197072044delinsAAT , CM000663.1:g.197072042_197072044delinsAAT	GRCh37
NC_000001.9:g.195338665_195338667delinsAAT	NCBI36
NG_015867.1:g.48781_48783delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6750_2108-6748delinsATT
ENST00000367409.9:c.6337_6339delinsATT MANE Select	ENSP00000356379.4:p.Ile2113=
ENST00000680265.1:c.6337_6339delinsATT	ENSP00000505384.1:p.Ile2113=
ENST00000680710.1:c.6337_6339delinsATT	ENSP00000506676.1:p.Ile2113=
ENST00000294732.11:c.4066-6750_4066-6748delinsATT	ENSP00000294732.7:n.4066-6750_4066-6748delinsATT
ENST00000367408.5:c.1816-6750_1816-6748delinsATT	ENSP00000356378.1:n.1816-6750_1816-6748delinsATT
ENST00000367409.8:c.6337_6339delinsATT	ENSP00000356379.4:p.Ile2113=
ENST00000612785.1:c.562-267_562-265delinsATT	ENSP00000479244.1:n.562-267_562-265delinsATT
NM_001206846.1:c.4066-6750_4066-6748delinsATT	NP_001193775.1:n.4066-6750_4066-6748delinsATT
NM_018136.4:c.6337_6339delinsATT	NP_060606.3:p.Ile2113=
NM_018136.5:c.6337_6339delinsATT MANE Select	NP_060606.3:p.Ile2113=
NM_001206846.2:c.4066-6750_4066-6748delinsATT	NP_001193775.1:n.4066-6750_4066-6748delinsATT