Canonical Allele Identifier: CA2535039375

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117710_197117711insG , CM000663.2:g.197117710_197117711insG	GRCh38
NC_000001.10:g.197086840_197086841insG , CM000663.1:g.197086840_197086841insG	GRCh37
NC_000001.9:g.195353463_195353464insG	NCBI36
NG_015867.1:g.33984_33985insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2107+78_2107+79insC
ENST00000367409.9:c.4065+78_4065+79insC MANE Select	ENSP00000356379.4:n.4065+78_4065+79insC
ENST00000680265.1:c.4065+78_4065+79insC	ENSP00000505384.1:n.4065+78_4065+79insC
ENST00000680710.1:c.4065+78_4065+79insC	ENSP00000506676.1:n.4065+78_4065+79insC
ENST00000681879.1:c.4113+78_4113+79insC	ENSP00000505363.1:n.4113+78_4113+79insC
ENST00000294732.11:c.4065+78_4065+79insC	ENSP00000294732.7:n.4065+78_4065+79insC
ENST00000367408.5:c.1815+78_1815+79insC	ENSP00000356378.1:n.1815+78_1815+79insC
ENST00000367409.8:c.4065+78_4065+79insC	ENSP00000356379.4:n.4065+78_4065+79insC
ENST00000612785.1:c.562-15064_562-15063insC	ENSP00000479244.1:n.562-15064_562-15063insC
NM_001206846.1:c.4065+78_4065+79insC	NP_001193775.1:n.4065+78_4065+79insC
NM_018136.4:c.4065+78_4065+79insC	NP_060606.3:n.4065+78_4065+79insC
NM_018136.5:c.4065+78_4065+79insC MANE Select	NP_060606.3:n.4065+78_4065+79insC
NM_001206846.2:c.4065+78_4065+79insC	NP_001193775.1:n.4065+78_4065+79insC