Canonical Allele Identifier: CA2586967849
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197139851dup , CM000663.2:g.197139851dup GRCh38
NC_000001.10:g.197108981dup , CM000663.1:g.197108981dup GRCh37
NC_000001.9:g.195375604dup NCBI36
NG_015867.1:g.11845dup

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1943dup MANE Select ENSP00000356379.4:p.Ile649AsnfsTer3
ENST00000679766.1:n.2160dup
ENST00000680265.1:c.1943dup ENSP00000505384.1:p.Ile649AsnfsTer3
ENST00000680710.1:c.1943dup ENSP00000506676.1:p.Ile649AsnfsTer3
ENST00000681879.1:c.1943dup ENSP00000505363.1:p.Ile649AsnfsTer3
ENST00000294732.11:c.1943dup ENSP00000294732.7:p.Ile649AsnfsTer3
ENST00000367409.8:c.1943dup ENSP00000356379.4:p.Ile649AsnfsTer3
ENST00000612785.1:c.561+3841dup ENSP00000479244.1:n.561+3841dup
NM_001206846.1:c.1943dup NP_001193775.1:p.Ile649AsnfsTer3
NM_018136.4:c.1943dup NP_060606.3:p.Ile649AsnfsTer3
NM_018136.5:c.1943dup MANE Select NP_060606.3:p.Ile649AsnfsTer3
NM_001206846.2:c.1943dup NP_001193775.1:p.Ile649AsnfsTer3