Canonical Allele Identifier: CA342262
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 21592
ClinVar RCV Id: RCV000020782
dbSNP Id: rs199422134

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197143675G>A , CM000663.2:g.197143675G>A GRCh38
NC_000001.10:g.197112805G>A , CM000663.1:g.197112805G>A GRCh37
NC_000001.9:g.195379428G>A NCBI36
NG_015867.1:g.8020C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.577C>T MANE Select ENSP00000356379.4:p.Gln193Ter
ENST00000679766.1:n.794C>T
ENST00000680265.1:c.577C>T ENSP00000505384.1:p.Gln193Ter
ENST00000680710.1:c.577C>T ENSP00000506676.1:p.Gln193Ter
ENST00000681879.1:c.577C>T ENSP00000505363.1:p.Gln193Ter
ENST00000294732.11:c.577C>T ENSP00000294732.7:p.Gln193Ter
ENST00000367409.8:c.577C>T ENSP00000356379.4:p.Gln193Ter
ENST00000612785.1:c.561+16C>T ENSP00000479244.1:n.561+16C>T
NM_001206846.1:c.577C>T NP_001193775.1:p.Gln193Ter
NM_018136.4:c.577C>T NP_060606.3:p.Gln193Ter
NM_018136.5:c.577C>T MANE Select NP_060606.3:p.Gln193Ter
NM_001206846.2:c.577C>T NP_001193775.1:p.Gln193Ter