Canonical Allele Identifier: CA1217930462
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197102896C= , CM000663.2:g.197102896C= GRCh38
NC_000001.10:g.197072026C= , CM000663.1:g.197072026C= GRCh37
NC_000001.9:g.195338649C= NCBI36
NG_015867.1:g.48799G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-6732G=
ENST00000367409.9:c.6355G= MANE Select ENSP00000356379.4:p.Ala2119=
ENST00000680265.1:c.6355G= ENSP00000505384.1:p.Ala2119=
ENST00000680710.1:c.6355G= ENSP00000506676.1:p.Ala2119=
ENST00000294732.11:c.4066-6732G= ENSP00000294732.7:n.4066-6732G=
ENST00000367408.5:c.1816-6732G= ENSP00000356378.1:n.1816-6732G=
ENST00000367409.8:c.6355G= ENSP00000356379.4:p.Ala2119=
ENST00000612785.1:c.562-249G= ENSP00000479244.1:n.562-249G=
NM_001206846.1:c.4066-6732G= NP_001193775.1:n.4066-6732G=
NM_018136.4:c.6355G= NP_060606.3:p.Ala2119=
NM_018136.5:c.6355G= MANE Select NP_060606.3:p.Ala2119=
NM_001206846.2:c.4066-6732G= NP_001193775.1:n.4066-6732G=