Canonical Allele Identifier: CA2747239546
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197088506_197088507insCCAAACACACCC , CM000663.2:g.197088506_197088507insCCAAACACACCC GRCh38
NC_000001.10:g.197057636_197057637insCCAAACACACCC , CM000663.1:g.197057636_197057637insCCAAACACACCC GRCh37
NC_000001.9:g.195324259_195324260insCCAAACACACCC NCBI36
NG_015867.1:g.63188_63189insGGGTGTGTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.3272-75_3272-74insGGGTGTGTTTGG
ENST00000367409.9:c.9985-75_9985-74insGGGTGTGTTTGG MANE Select ENSP00000356379.4:n.9985-75_9985-74insGGGTGTGTTTGG
ENST00000680265.1:c.10207-75_10207-74insGGGTGTGTTTGG ENSP00000505384.1:n.10207-75_10207-74insGGGTGTGTTTGG
ENST00000680710.1:c.9961-75_9961-74insGGGTGTGTTTGG ENSP00000506676.1:n.9961-75_9961-74insGGGTGTGTTTGG
ENST00000294732.11:c.5230-75_5230-74insGGGTGTGTTTGG ENSP00000294732.7:n.5230-75_5230-74insGGGTGTGTTTGG
ENST00000367408.5:c.2980-75_2980-74insGGGTGTGTTTGG ENSP00000356378.1:n.2980-75_2980-74insGGGTGTGTTTGG
ENST00000367409.8:c.9985-75_9985-74insGGGTGTGTTTGG ENSP00000356379.4:n.9985-75_9985-74insGGGTGTGTTTGG
ENST00000612785.1:c.3943-75_3943-74insGGGTGTGTTTGG ENSP00000479244.1:n.3943-75_3943-74insGGGTGTGTTTGG
NM_001206846.1:c.5230-75_5230-74insGGGTGTGTTTGG NP_001193775.1:n.5230-75_5230-74insGGGTGTGTTTGG
NM_018136.4:c.9985-75_9985-74insGGGTGTGTTTGG NP_060606.3:n.9985-75_9985-74insGGGTGTGTTTGG
NM_018136.5:c.9985-75_9985-74insGGGTGTGTTTGG MANE Select NP_060606.3:n.9985-75_9985-74insGGGTGTGTTTGG
NM_001206846.2:c.5230-75_5230-74insGGGTGTGTTTGG NP_001193775.1:n.5230-75_5230-74insGGGTGTGTTTGG