Canonical Allele Identifier: CA729743266
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs1469620788

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197091042_197091043del , CM000663.2:g.197091042_197091043del GRCh38
NC_000001.10:g.197060172_197060173del , CM000663.1:g.197060172_197060173del GRCh37
NC_000001.9:g.195326795_195326796del NCBI36
NG_015867.1:g.60655_60656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2733_2734del
ENST00000367409.9:c.9446_9447del
ENST00000680265.1:c.9668_9669del
ENST00000680710.1:c.9422_9423del
ENST00000294732.11:c.4691_4692del
ENST00000367408.5:c.2441_2442del
ENST00000367409.8:c.9446_9447del
ENST00000612785.1:c.3404_3405del
NM_001206846.1:c.4691_4692del
NM_018136.4:c.9446_9447del
NM_018136.5:c.9446_9447del
NM_001206846.2:c.4691_4692del