Canonical Allele Identifier: CA1217923380
Gene: ASPM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197088147A= , CM000663.2:g.197088147A= GRCh38
NC_000001.10:g.197057277A= , CM000663.1:g.197057277A= GRCh37
NC_000001.9:g.195323900A= NCBI36
NG_015867.1:g.63548T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.3448+109T=
ENST00000367409.9:c.10161+109T= MANE Select ENSP00000356379.4:n.10161+109T=
ENST00000680265.1:c.10383+109T= ENSP00000505384.1:n.10383+109T=
ENST00000680710.1:c.10137+109T= ENSP00000506676.1:n.10137+109T=
ENST00000294732.11:c.5406+109T= ENSP00000294732.7:n.5406+109T=
ENST00000367408.5:c.3156+109T= ENSP00000356378.1:n.3156+109T=
ENST00000367409.8:c.10161+109T= ENSP00000356379.4:n.10161+109T=
NM_001206846.1:c.5406+109T= NP_001193775.1:n.5406+109T=
NM_018136.4:c.10161+109T= NP_060606.3:n.10161+109T=
NM_018136.5:c.10161+109T= MANE Select NP_060606.3:n.10161+109T=
NM_001206846.2:c.5406+109T= NP_001193775.1:n.5406+109T=
Search 100 bp 5'
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