Canonical Allele Identifier: CA1143732118
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197102988T= , CM000663.2:g.197102988T= GRCh38
NC_000001.10:g.197072118T= , CM000663.1:g.197072118T= GRCh37
NC_000001.9:g.195338741T= NCBI36
NG_015867.1:g.48707A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-6824A=
ENST00000367409.9:c.6263A= MANE Select ENSP00000356379.4:p.Lys2088=
ENST00000680265.1:c.6263A= ENSP00000505384.1:p.Lys2088=
ENST00000680710.1:c.6263A= ENSP00000506676.1:p.Lys2088=
ENST00000294732.11:c.4066-6824A= ENSP00000294732.7:n.4066-6824A=
ENST00000367408.5:c.1816-6824A= ENSP00000356378.1:n.1816-6824A=
ENST00000367409.8:c.6263A= ENSP00000356379.4:p.Lys2088=
ENST00000612785.1:c.562-341A= ENSP00000479244.1:n.562-341A=
NM_001206846.1:c.4066-6824A= NP_001193775.1:n.4066-6824A=
NM_018136.4:c.6263A= NP_060606.3:p.Lys2088=
NM_018136.5:c.6263A= MANE Select NP_060606.3:p.Lys2088=
NM_001206846.2:c.4066-6824A= NP_001193775.1:n.4066-6824A=