Canonical Allele Identifier: CA2558458819

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093015_197093016insC , CM000663.2:g.197093015_197093016insC	GRCh38
NC_000001.10:g.197062145_197062146insC , CM000663.1:g.197062145_197062146insC	GRCh37
NC_000001.9:g.195328768_195328769insC	NCBI36
NG_015867.1:g.58679_58680insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2581+36_2581+37insG
ENST00000367409.9:c.9294+36_9294+37insG MANE Select	ENSP00000356379.4:n.9294+36_9294+37insG
ENST00000680265.1:c.9516+36_9516+37insG	ENSP00000505384.1:n.9516+36_9516+37insG
ENST00000680710.1:c.9294+36_9294+37insG	ENSP00000506676.1:n.9294+36_9294+37insG
ENST00000294732.11:c.4539+36_4539+37insG	ENSP00000294732.7:n.4539+36_4539+37insG
ENST00000367408.5:c.2289+36_2289+37insG	ENSP00000356378.1:n.2289+36_2289+37insG
ENST00000367409.8:c.9294+36_9294+37insG	ENSP00000356379.4:n.9294+36_9294+37insG
ENST00000612785.1:c.3252+36_3252+37insG	ENSP00000479244.1:n.3252+36_3252+37insG
NM_001206846.1:c.4539+36_4539+37insG	NP_001193775.1:n.4539+36_4539+37insG
NM_018136.4:c.9294+36_9294+37insG	NP_060606.3:n.9294+36_9294+37insG
NM_018136.5:c.9294+36_9294+37insG MANE Select	NP_060606.3:n.9294+36_9294+37insG
NM_001206846.2:c.4539+36_4539+37insG	NP_001193775.1:n.4539+36_4539+37insG