Canonical Allele Identifier: CA1217926657

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093026_197093027delinsGA , CM000663.2:g.197093026_197093027delinsGA	GRCh38
NC_000001.10:g.197062156_197062157delinsGA , CM000663.1:g.197062156_197062157delinsGA	GRCh37
NC_000001.9:g.195328779_195328780delinsGA	NCBI36
NG_015867.1:g.58668_58669delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2581+25_2581+26delinsTC
ENST00000367409.9:c.9294+25_9294+26delinsTC MANE Select	ENSP00000356379.4:n.9294+25_9294+26delinsTC
ENST00000680265.1:c.9516+25_9516+26delinsTC	ENSP00000505384.1:n.9516+25_9516+26delinsTC
ENST00000680710.1:c.9294+25_9294+26delinsTC	ENSP00000506676.1:n.9294+25_9294+26delinsTC
ENST00000294732.11:c.4539+25_4539+26delinsTC	ENSP00000294732.7:n.4539+25_4539+26delinsTC
ENST00000367408.5:c.2289+25_2289+26delinsTC	ENSP00000356378.1:n.2289+25_2289+26delinsTC
ENST00000367409.8:c.9294+25_9294+26delinsTC	ENSP00000356379.4:n.9294+25_9294+26delinsTC
ENST00000612785.1:c.3252+25_3252+26delinsTC	ENSP00000479244.1:n.3252+25_3252+26delinsTC
NM_001206846.1:c.4539+25_4539+26delinsTC	NP_001193775.1:n.4539+25_4539+26delinsTC
NM_018136.4:c.9294+25_9294+26delinsTC	NP_060606.3:n.9294+25_9294+26delinsTC
NM_018136.5:c.9294+25_9294+26delinsTC MANE Select	NP_060606.3:n.9294+25_9294+26delinsTC
NM_001206846.2:c.4539+25_4539+26delinsTC	NP_001193775.1:n.4539+25_4539+26delinsTC