Canonical Allele Identifier: CA344014958
Gene: ASPM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142579T>A , CM000663.2:g.197142579T>A GRCh38
NC_000001.10:g.197111709T>A , CM000663.1:g.197111709T>A GRCh37
NC_000001.9:g.195378332T>A NCBI36
NG_015867.1:g.9116A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1673A>T MANE Select ENSP00000356379.4:p.Tyr558Phe
ENST00000679766.1:n.1890A>T
ENST00000680265.1:c.1673A>T ENSP00000505384.1:p.Tyr558Phe
ENST00000680710.1:c.1673A>T ENSP00000506676.1:p.Tyr558Phe
ENST00000681879.1:c.1673A>T ENSP00000505363.1:p.Tyr558Phe
ENST00000294732.11:c.1673A>T ENSP00000294732.7:p.Tyr558Phe
ENST00000367409.8:c.1673A>T ENSP00000356379.4:p.Tyr558Phe
ENST00000612785.1:c.561+1112A>T ENSP00000479244.1:n.561+1112A>T
NM_001206846.1:c.1673A>T NP_001193775.1:p.Tyr558Phe
NM_018136.4:c.1673A>T NP_060606.3:p.Tyr558Phe
NM_018136.5:c.1673A>T MANE Select NP_060606.3:p.Tyr558Phe
NM_001206846.2:c.1673A>T NP_001193775.1:p.Tyr558Phe