Canonical Allele Identifier: CA1217925451

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090587_197090588delinsAC , CM000663.2:g.197090587_197090588delinsAC	GRCh38
NC_000001.10:g.197059717_197059718delinsAC , CM000663.1:g.197059717_197059718delinsAC	GRCh37
NC_000001.9:g.195326340_195326341delinsAC	NCBI36
NG_015867.1:g.61107_61108delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2924-200_2924-199delinsGT
ENST00000367409.9:c.9637-200_9637-199delinsGT MANE Select	ENSP00000356379.4:n.9637-200_9637-199delinsGT
ENST00000680265.1:c.9859-200_9859-199delinsGT	ENSP00000505384.1:n.9859-200_9859-199delinsGT
ENST00000680710.1:c.9613-200_9613-199delinsGT	ENSP00000506676.1:n.9613-200_9613-199delinsGT
ENST00000294732.11:c.4882-200_4882-199delinsGT	ENSP00000294732.7:n.4882-200_4882-199delinsGT
ENST00000367408.5:c.2632-200_2632-199delinsGT	ENSP00000356378.1:n.2632-200_2632-199delinsGT
ENST00000367409.8:c.9637-200_9637-199delinsGT	ENSP00000356379.4:n.9637-200_9637-199delinsGT
ENST00000612785.1:c.3595-200_3595-199delinsGT	ENSP00000479244.1:n.3595-200_3595-199delinsGT
NM_001206846.1:c.4882-200_4882-199delinsGT	NP_001193775.1:n.4882-200_4882-199delinsGT
NM_018136.4:c.9637-200_9637-199delinsGT	NP_060606.3:n.9637-200_9637-199delinsGT
NM_018136.5:c.9637-200_9637-199delinsGT MANE Select	NP_060606.3:n.9637-200_9637-199delinsGT
NM_001206846.2:c.4882-200_4882-199delinsGT	NP_001193775.1:n.4882-200_4882-199delinsGT