Canonical Allele Identifier: CA1217946324

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197141949_197141950delinsAG , CM000663.2:g.197141949_197141950delinsAG	GRCh38
NC_000001.10:g.197111079_197111080delinsAG , CM000663.1:g.197111079_197111080delinsAG	GRCh37
NC_000001.9:g.195377702_195377703delinsAG	NCBI36
NG_015867.1:g.9745_9746delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1921+381_1921+382delinsCT MANE Select	ENSP00000356379.4:n.1921+381_1921+382delinsCT
ENST00000679766.1:n.2138+381_2138+382delinsCT
ENST00000680265.1:c.1921+381_1921+382delinsCT	ENSP00000505384.1:n.1921+381_1921+382delinsCT
ENST00000680710.1:c.1921+381_1921+382delinsCT	ENSP00000506676.1:n.1921+381_1921+382delinsCT
ENST00000681879.1:c.1921+381_1921+382delinsCT	ENSP00000505363.1:n.1921+381_1921+382delinsCT
ENST00000294732.11:c.1921+381_1921+382delinsCT	ENSP00000294732.7:n.1921+381_1921+382delinsCT
ENST00000367409.8:c.1921+381_1921+382delinsCT	ENSP00000356379.4:n.1921+381_1921+382delinsCT
ENST00000612785.1:c.561+1741_561+1742delinsCT	ENSP00000479244.1:n.561+1741_561+1742delinsCT
NM_001206846.1:c.1921+381_1921+382delinsCT	NP_001193775.1:n.1921+381_1921+382delinsCT
NM_018136.4:c.1921+381_1921+382delinsCT	NP_060606.3:n.1921+381_1921+382delinsCT
NM_018136.5:c.1921+381_1921+382delinsCT MANE Select	NP_060606.3:n.1921+381_1921+382delinsCT
NM_001206846.2:c.1921+381_1921+382delinsCT	NP_001193775.1:n.1921+381_1921+382delinsCT