Canonical Allele Identifier: CA1217923666

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088515_197088516delinsAG , CM000663.2:g.197088515_197088516delinsAG	GRCh38
NC_000001.10:g.197057645_197057646delinsAG , CM000663.1:g.197057645_197057646delinsAG	GRCh37
NC_000001.9:g.195324268_195324269delinsAG	NCBI36
NG_015867.1:g.63179_63180delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3272-84_3272-83delinsCT
ENST00000367409.9:c.9985-84_9985-83delinsCT MANE Select	ENSP00000356379.4:n.9985-84_9985-83delinsCT
ENST00000680265.1:c.10207-84_10207-83delinsCT	ENSP00000505384.1:n.10207-84_10207-83delinsCT
ENST00000680710.1:c.9961-84_9961-83delinsCT	ENSP00000506676.1:n.9961-84_9961-83delinsCT
ENST00000294732.11:c.5230-84_5230-83delinsCT	ENSP00000294732.7:n.5230-84_5230-83delinsCT
ENST00000367408.5:c.2980-84_2980-83delinsCT	ENSP00000356378.1:n.2980-84_2980-83delinsCT
ENST00000367409.8:c.9985-84_9985-83delinsCT	ENSP00000356379.4:n.9985-84_9985-83delinsCT
ENST00000612785.1:c.3943-84_3943-83delinsCT	ENSP00000479244.1:n.3943-84_3943-83delinsCT
NM_001206846.1:c.5230-84_5230-83delinsCT	NP_001193775.1:n.5230-84_5230-83delinsCT
NM_018136.4:c.9985-84_9985-83delinsCT	NP_060606.3:n.9985-84_9985-83delinsCT
NM_018136.5:c.9985-84_9985-83delinsCT MANE Select	NP_060606.3:n.9985-84_9985-83delinsCT
NM_001206846.2:c.5230-84_5230-83delinsCT	NP_001193775.1:n.5230-84_5230-83delinsCT