Canonical Allele Identifier: CA1309800
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs772469520

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197104079C>A , CM000663.2:g.197104079C>A GRCh38
NC_000001.10:g.197073209C>A , CM000663.1:g.197073209C>A GRCh37
NC_000001.9:g.195339832C>A NCBI36
NG_015867.1:g.47616G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-7915G>T
ENST00000367409.9:c.5172G>T MANE Select ENSP00000356379.4:p.Glu1724Asp
ENST00000680265.1:c.5172G>T ENSP00000505384.1:p.Glu1724Asp
ENST00000680710.1:c.5172G>T ENSP00000506676.1:p.Glu1724Asp
ENST00000294732.11:c.4066-7915G>T ENSP00000294732.7:n.4066-7915G>T
ENST00000367408.5:c.1816-7915G>T ENSP00000356378.1:n.1816-7915G>T
ENST00000367409.8:c.5172G>T ENSP00000356379.4:p.Glu1724Asp
ENST00000612785.1:c.562-1432G>T ENSP00000479244.1:n.562-1432G>T
NM_001206846.1:c.4066-7915G>T NP_001193775.1:n.4066-7915G>T
NM_018136.4:c.5172G>T NP_060606.3:p.Glu1724Asp
NM_018136.5:c.5172G>T MANE Select NP_060606.3:p.Glu1724Asp
NM_001206846.2:c.4066-7915G>T NP_001193775.1:n.4066-7915G>T