Canonical Allele Identifier: CA1217945357
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142524_197142526delinsCTT , CM000663.2:g.197142524_197142526delinsCTT GRCh38
NC_000001.10:g.197111654_197111656delinsCTT , CM000663.1:g.197111654_197111656delinsCTT GRCh37
NC_000001.9:g.195378277_195378279delinsCTT NCBI36
NG_015867.1:g.9169_9171delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367409.9:c.1726_1728delinsAAG MANE Select ENSP00000356379.4:p.Lys576=
ENST00000679766.1:n.1943_1945delinsAAG
ENST00000680265.1:c.1726_1728delinsAAG ENSP00000505384.1:p.Lys576=
ENST00000680710.1:c.1726_1728delinsAAG ENSP00000506676.1:p.Lys576=
ENST00000681879.1:c.1726_1728delinsAAG ENSP00000505363.1:p.Lys576=
ENST00000294732.11:c.1726_1728delinsAAG ENSP00000294732.7:p.Lys576=
ENST00000367409.8:c.1726_1728delinsAAG ENSP00000356379.4:p.Lys576=
ENST00000612785.1:c.561+1165_561+1167delinsAAG ENSP00000479244.1:n.561+1165_561+1167delinsAAG
NM_001206846.1:c.1726_1728delinsAAG NP_001193775.1:p.Lys576=
NM_018136.4:c.1726_1728delinsAAG NP_060606.3:p.Lys576=
NM_018136.5:c.1726_1728delinsAAG MANE Select NP_060606.3:p.Lys576=
NM_001206846.2:c.1726_1728delinsAAG NP_001193775.1:p.Lys576=