Canonical Allele Identifier: CA1217930964

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197104186_197104187delinsCA , CM000663.2:g.197104186_197104187delinsCA	GRCh38
NC_000001.10:g.197073316_197073317delinsCA , CM000663.1:g.197073316_197073317delinsCA	GRCh37
NC_000001.9:g.195339939_195339940delinsCA	NCBI36
NG_015867.1:g.47508_47509delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-8023_2108-8022delinsTG
ENST00000367409.9:c.5064_5065delinsTG MANE Select	ENSP00000356379.4:p.Thr1688=
ENST00000680265.1:c.5064_5065delinsTG	ENSP00000505384.1:p.Thr1688=
ENST00000680710.1:c.5064_5065delinsTG	ENSP00000506676.1:p.Thr1688=
ENST00000294732.11:c.4066-8023_4066-8022delinsTG	ENSP00000294732.7:n.4066-8023_4066-8022delinsTG
ENST00000367408.5:c.1816-8023_1816-8022delinsTG	ENSP00000356378.1:n.1816-8023_1816-8022delinsTG
ENST00000367409.8:c.5064_5065delinsTG	ENSP00000356379.4:p.Thr1688=
ENST00000612785.1:c.562-1540_562-1539delinsTG	ENSP00000479244.1:n.562-1540_562-1539delinsTG
NM_001206846.1:c.4066-8023_4066-8022delinsTG	NP_001193775.1:n.4066-8023_4066-8022delinsTG
NM_018136.4:c.5064_5065delinsTG	NP_060606.3:p.Thr1688=
NM_018136.5:c.5064_5065delinsTG MANE Select	NP_060606.3:p.Thr1688=
NM_001206846.2:c.4066-8023_4066-8022delinsTG	NP_001193775.1:n.4066-8023_4066-8022delinsTG