Canonical Allele Identifier: CA1217930481

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102942_197102944delinsAAC , CM000663.2:g.197102942_197102944delinsAAC	GRCh38
NC_000001.10:g.197072072_197072074delinsAAC , CM000663.1:g.197072072_197072074delinsAAC	GRCh37
NC_000001.9:g.195338695_195338697delinsAAC	NCBI36
NG_015867.1:g.48751_48753delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6780_2108-6778delinsGTT
ENST00000367409.9:c.6307_6309delinsGTT MANE Select	ENSP00000356379.4:p.Val2103=
ENST00000680265.1:c.6307_6309delinsGTT	ENSP00000505384.1:p.Val2103=
ENST00000680710.1:c.6307_6309delinsGTT	ENSP00000506676.1:p.Val2103=
ENST00000294732.11:c.4066-6780_4066-6778delinsGTT	ENSP00000294732.7:n.4066-6780_4066-6778delinsGTT
ENST00000367408.5:c.1816-6780_1816-6778delinsGTT	ENSP00000356378.1:n.1816-6780_1816-6778delinsGTT
ENST00000367409.8:c.6307_6309delinsGTT	ENSP00000356379.4:p.Val2103=
ENST00000612785.1:c.562-297_562-295delinsGTT	ENSP00000479244.1:n.562-297_562-295delinsGTT
NM_001206846.1:c.4066-6780_4066-6778delinsGTT	NP_001193775.1:n.4066-6780_4066-6778delinsGTT
NM_018136.4:c.6307_6309delinsGTT	NP_060606.3:p.Val2103=
NM_018136.5:c.6307_6309delinsGTT MANE Select	NP_060606.3:p.Val2103=
NM_001206846.2:c.4066-6780_4066-6778delinsGTT	NP_001193775.1:n.4066-6780_4066-6778delinsGTT