Canonical Allele Identifier: CA1217923337
Gene: ASPM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197088105T= , CM000663.2:g.197088105T= GRCh38
NC_000001.10:g.197057235T= , CM000663.1:g.197057235T= GRCh37
NC_000001.9:g.195323858T= NCBI36
NG_015867.1:g.63590A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.3448+151A=
ENST00000367409.9:c.10161+151A= MANE Select ENSP00000356379.4:n.10161+151A=
ENST00000680265.1:c.10383+151A= ENSP00000505384.1:n.10383+151A=
ENST00000680710.1:c.10137+151A= ENSP00000506676.1:n.10137+151A=
ENST00000294732.11:c.5406+151A= ENSP00000294732.7:n.5406+151A=
ENST00000367408.5:c.3156+151A= ENSP00000356378.1:n.3156+151A=
ENST00000367409.8:c.10161+151A= ENSP00000356379.4:n.10161+151A=
NM_001206846.1:c.5406+151A= NP_001193775.1:n.5406+151A=
NM_018136.4:c.10161+151A= NP_060606.3:n.10161+151A=
NM_018136.5:c.10161+151A= MANE Select NP_060606.3:n.10161+151A=
NM_001206846.2:c.5406+151A= NP_001193775.1:n.5406+151A=
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