Canonical Allele Identifier: CA342285
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21618
ClinVar RCV Id: RCV000020808
dbSNP Id: rs199422181

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197100583G>A , CM000663.2:g.197100583G>A GRCh38
NC_000001.10:g.197069713G>A , CM000663.1:g.197069713G>A GRCh37
NC_000001.9:g.195336336G>A NCBI36
NG_015867.1:g.51112C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-4419C>T
ENST00000367409.9:c.8668C>T MANE Select ENSP00000356379.4:p.Gln2890Ter
ENST00000680265.1:c.8668C>T ENSP00000505384.1:p.Gln2890Ter
ENST00000680710.1:c.8668C>T ENSP00000506676.1:p.Gln2890Ter
ENST00000294732.11:c.4066-4419C>T ENSP00000294732.7:n.4066-4419C>T
ENST00000367408.5:c.1816-4419C>T ENSP00000356378.1:n.1816-4419C>T
ENST00000367409.8:c.8668C>T ENSP00000356379.4:p.Gln2890Ter
ENST00000612785.1:c.2626C>T ENSP00000479244.1:p.Gln876Ter
NM_001206846.1:c.4066-4419C>T NP_001193775.1:n.4066-4419C>T
NM_018136.4:c.8668C>T NP_060606.3:p.Gln2890Ter
NM_018136.5:c.8668C>T MANE Select NP_060606.3:p.Gln2890Ter
NM_001206846.2:c.4066-4419C>T NP_001193775.1:n.4066-4419C>T