Canonical Allele Identifier: CA1217929985
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101585_197101587delinsCTT , CM000663.2:g.197101585_197101587delinsCTT GRCh38
NC_000001.10:g.197070715_197070717delinsCTT , CM000663.1:g.197070715_197070717delinsCTT GRCh37
NC_000001.9:g.195337338_195337340delinsCTT NCBI36
NG_015867.1:g.50108_50110delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-5423_2108-5421delinsAAG
ENST00000367409.9:c.7664_7666delinsAAG MANE Select ENSP00000356379.4:p.Lys2555=
ENST00000680265.1:c.7664_7666delinsAAG ENSP00000505384.1:p.Lys2555=
ENST00000680710.1:c.7664_7666delinsAAG ENSP00000506676.1:p.Lys2555=
ENST00000294732.11:c.4066-5423_4066-5421delinsAAG ENSP00000294732.7:n.4066-5423_4066-5421de...
ENST00000367408.5:c.1816-5423_1816-5421delinsAAG ENSP00000356378.1:n.1816-5423_1816-5421de...
ENST00000367409.8:c.7664_7666delinsAAG ENSP00000356379.4:p.Lys2555=
ENST00000612785.1:c.1622_1624delinsAAG ENSP00000479244.1:p.Lys541=
NM_001206846.1:c.4066-5423_4066-5421delinsAAG NP_001193775.1:n.4066-5423_4066-5421delin...
NM_018136.4:c.7664_7666delinsAAG NP_060606.3:p.Lys2555=
NM_018136.5:c.7664_7666delinsAAG MANE Select NP_060606.3:p.Lys2555=
NM_001206846.2:c.4066-5423_4066-5421delinsAAG NP_001193775.1:n.4066-5423_4066-5421delin...