Canonical Allele Identifier: CA1217926720
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197093188T= , CM000663.2:g.197093188T= GRCh38
NC_000001.10:g.197062318T= , CM000663.1:g.197062318T= GRCh37
NC_000001.9:g.195328941T= NCBI36
NG_015867.1:g.58507A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2445A=
ENST00000367409.9:c.9158A= MANE Select ENSP00000356379.4:p.Lys3053=
ENST00000680265.1:c.9380A= ENSP00000505384.1:p.Lys3127=
ENST00000680710.1:c.9158A= ENSP00000506676.1:p.Lys3053=
ENST00000294732.11:c.4403A= ENSP00000294732.7:p.Lys1468=
ENST00000367408.5:c.2153A= ENSP00000356378.1:p.Lys718=
ENST00000367409.8:c.9158A= ENSP00000356379.4:p.Lys3053=
ENST00000612785.1:c.3116A= ENSP00000479244.1:p.Lys1039=
NM_001206846.1:c.4403A= NP_001193775.1:p.Lys1468=
NM_018136.4:c.9158A= NP_060606.3:p.Lys3053=
NM_018136.5:c.9158A= MANE Select NP_060606.3:p.Lys3053=
NM_001206846.2:c.4403A= NP_001193775.1:p.Lys1468=