Canonical Allele Identifier: CA1217945281
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142492C= , CM000663.2:g.197142492C= GRCh38
NC_000001.10:g.197111622C= , CM000663.1:g.197111622C= GRCh37
NC_000001.9:g.195378245C= NCBI36
NG_015867.1:g.9203G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1760G= MANE Select ENSP00000356379.4:p.Arg587=
ENST00000679766.1:n.1977G=
ENST00000680265.1:c.1760G= ENSP00000505384.1:p.Arg587=
ENST00000680710.1:c.1760G= ENSP00000506676.1:p.Arg587=
ENST00000681879.1:c.1760G= ENSP00000505363.1:p.Arg587=
ENST00000294732.11:c.1760G= ENSP00000294732.7:p.Arg587=
ENST00000367409.8:c.1760G= ENSP00000356379.4:p.Arg587=
ENST00000612785.1:c.561+1199G= ENSP00000479244.1:n.561+1199G=
NM_001206846.1:c.1760G= NP_001193775.1:p.Arg587=
NM_018136.4:c.1760G= NP_060606.3:p.Arg587=
NM_018136.5:c.1760G= MANE Select NP_060606.3:p.Arg587=
NM_001206846.2:c.1760G= NP_001193775.1:p.Arg587=