Canonical Allele Identifier: CA1217923708

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088579_197088581delinsTAG , CM000663.2:g.197088579_197088581delinsTAG	GRCh38
NC_000001.10:g.197057709_197057711delinsTAG , CM000663.1:g.197057709_197057711delinsTAG	GRCh37
NC_000001.9:g.195324332_195324334delinsTAG	NCBI36
NG_015867.1:g.63114_63116delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3272-149_3272-147delinsCTA
ENST00000367409.9:c.9985-149_9985-147delinsCTA MANE Select	ENSP00000356379.4:n.9985-149_9985-147delinsCTA
ENST00000680265.1:c.10207-149_10207-147delinsCTA	ENSP00000505384.1:n.10207-149_10207-147delinsCTA
ENST00000680710.1:c.9961-149_9961-147delinsCTA	ENSP00000506676.1:n.9961-149_9961-147delinsCTA
ENST00000294732.11:c.5230-149_5230-147delinsCTA	ENSP00000294732.7:n.5230-149_5230-147delinsCTA
ENST00000367408.5:c.2980-149_2980-147delinsCTA	ENSP00000356378.1:n.2980-149_2980-147delinsCTA
ENST00000367409.8:c.9985-149_9985-147delinsCTA	ENSP00000356379.4:n.9985-149_9985-147delinsCTA
ENST00000612785.1:c.3943-149_3943-147delinsCTA	ENSP00000479244.1:n.3943-149_3943-147delinsCTA
NM_001206846.1:c.5230-149_5230-147delinsCTA	NP_001193775.1:n.5230-149_5230-147delinsCTA
NM_018136.4:c.9985-149_9985-147delinsCTA	NP_060606.3:n.9985-149_9985-147delinsCTA
NM_018136.5:c.9985-149_9985-147delinsCTA MANE Select	NP_060606.3:n.9985-149_9985-147delinsCTA
NM_001206846.2:c.5230-149_5230-147delinsCTA	NP_001193775.1:n.5230-149_5230-147delinsCTA