Canonical Allele Identifier: CA1217930766

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103659_197103661delinsAAG , CM000663.2:g.197103659_197103661delinsAAG	GRCh38
NC_000001.10:g.197072789_197072791delinsAAG , CM000663.1:g.197072789_197072791delinsAAG	GRCh37
NC_000001.9:g.195339412_195339414delinsAAG	NCBI36
NG_015867.1:g.48034_48036delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7497_2108-7495delinsCTT
ENST00000367409.9:c.5590_5592delinsCTT MANE Select	ENSP00000356379.4:p.Leu1864=
ENST00000680265.1:c.5590_5592delinsCTT	ENSP00000505384.1:p.Leu1864=
ENST00000680710.1:c.5590_5592delinsCTT	ENSP00000506676.1:p.Leu1864=
ENST00000294732.11:c.4066-7497_4066-7495delinsCTT	ENSP00000294732.7:n.4066-7497_4066-7495delinsCTT
ENST00000367408.5:c.1816-7497_1816-7495delinsCTT	ENSP00000356378.1:n.1816-7497_1816-7495delinsCTT
ENST00000367409.8:c.5590_5592delinsCTT	ENSP00000356379.4:p.Leu1864=
ENST00000612785.1:c.562-1014_562-1012delinsCTT	ENSP00000479244.1:n.562-1014_562-1012delinsCTT
NM_001206846.1:c.4066-7497_4066-7495delinsCTT	NP_001193775.1:n.4066-7497_4066-7495delinsCTT
NM_018136.4:c.5590_5592delinsCTT	NP_060606.3:p.Leu1864=
NM_018136.5:c.5590_5592delinsCTT MANE Select	NP_060606.3:p.Leu1864=
NM_001206846.2:c.4066-7497_4066-7495delinsCTT	NP_001193775.1:n.4066-7497_4066-7495delinsCTT