Canonical Allele Identifier: CA1217938423
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197121930_197121932delinsATC , CM000663.2:g.197121930_197121932delinsATC GRCh38
NC_000001.10:g.197091060_197091062delinsATC , CM000663.1:g.197091060_197091062delinsATC GRCh37
NC_000001.9:g.195357683_195357685delinsATC NCBI36
NG_015867.1:g.29763_29765delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1895_1897delinsGAT
ENST00000367409.9:c.3853_3855delinsGAT MANE Select ENSP00000356379.4:p.Asp1285=
ENST00000680112.1:n.1909_1911delinsGAT
ENST00000680265.1:c.3853_3855delinsGAT ENSP00000505384.1:p.Asp1285=
ENST00000680710.1:c.3853_3855delinsGAT ENSP00000506676.1:p.Asp1285=
ENST00000681879.1:c.3853_3855delinsGAT ENSP00000505363.1:p.Asp1285=
ENST00000294732.11:c.3853_3855delinsGAT ENSP00000294732.7:p.Asp1285=
ENST00000367408.5:c.1603_1605delinsGAT ENSP00000356378.1:p.Asp535=
ENST00000367409.8:c.3853_3855delinsGAT ENSP00000356379.4:p.Asp1285=
ENST00000612785.1:c.562-19285_562-19283delinsGAT ENSP00000479244.1:n.562-19285_562-19283delinsGAT
NM_001206846.1:c.3853_3855delinsGAT NP_001193775.1:p.Asp1285=
NM_018136.4:c.3853_3855delinsGAT NP_060606.3:p.Asp1285=
NM_018136.5:c.3853_3855delinsGAT MANE Select NP_060606.3:p.Asp1285=
NM_001206846.2:c.3853_3855delinsGAT NP_001193775.1:p.Asp1285=