Canonical Allele Identifier: CA1309196
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs760223682

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197100667C>A , CM000663.2:g.197100667C>A GRCh38
NC_000001.10:g.197069797C>A , CM000663.1:g.197069797C>A GRCh37
NC_000001.9:g.195336420C>A NCBI36
NG_015867.1:g.51028G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-4503G>T
ENST00000367409.9:c.8584G>T MANE Select ENSP00000356379.4:p.Ala2862Ser
ENST00000680265.1:c.8584G>T ENSP00000505384.1:p.Ala2862Ser
ENST00000680710.1:c.8584G>T ENSP00000506676.1:p.Ala2862Ser
ENST00000294732.11:c.4066-4503G>T ENSP00000294732.7:n.4066-4503G>T
ENST00000367408.5:c.1816-4503G>T ENSP00000356378.1:n.1816-4503G>T
ENST00000367409.8:c.8584G>T ENSP00000356379.4:p.Ala2862Ser
ENST00000612785.1:c.2542G>T ENSP00000479244.1:p.Ala848Ser
NM_001206846.1:c.4066-4503G>T NP_001193775.1:n.4066-4503G>T
NM_018136.4:c.8584G>T NP_060606.3:p.Ala2862Ser
NM_018136.5:c.8584G>T MANE Select NP_060606.3:p.Ala2862Ser
NM_001206846.2:c.4066-4503G>T NP_001193775.1:n.4066-4503G>T