Canonical Allele Identifier: CA1217929809
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101114_197101118delinsTTTTC , CM000663.2:g.197101114_197101118delinsTTTTC GRCh38
NC_000001.10:g.197070244_197070248delinsTTTTC , CM000663.1:g.197070244_197070248delinsTTTTC GRCh37
NC_000001.9:g.195336867_195336871delinsTTTTC NCBI36
NG_015867.1:g.50577_50581delinsGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-4954_2108-4950delinsGAAAA
ENST00000367409.9:c.8133_8137delinsGAAAA MANE Select ENSP00000356379.4:p.Lys2711=
ENST00000680265.1:c.8133_8137delinsGAAAA ENSP00000505384.1:p.Lys2711=
ENST00000680710.1:c.8133_8137delinsGAAAA ENSP00000506676.1:p.Lys2711=
ENST00000294732.11:c.4066-4954_4066-4950delinsGAAAA ENSP00000294732.7:n.4066-4954_4066-4950delinsGAAAA
ENST00000367408.5:c.1816-4954_1816-4950delinsGAAAA ENSP00000356378.1:n.1816-4954_1816-4950delinsGAAAA
ENST00000367409.8:c.8133_8137delinsGAAAA ENSP00000356379.4:p.Lys2711=
ENST00000612785.1:c.2091_2095delinsGAAAA ENSP00000479244.1:p.Lys697=
NM_001206846.1:c.4066-4954_4066-4950delinsGAAAA NP_001193775.1:n.4066-4954_4066-4950delinsGAAAA
NM_018136.4:c.8133_8137delinsGAAAA NP_060606.3:p.Lys2711=
NM_018136.5:c.8133_8137delinsGAAAA MANE Select NP_060606.3:p.Lys2711=
NM_001206846.2:c.4066-4954_4066-4950delinsGAAAA NP_001193775.1:n.4066-4954_4066-4950delinsGAAAA