Canonical Allele Identifier: CA1217923303

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088066_197088070delinsGTTTC , CM000663.2:g.197088066_197088070delinsGTTTC	GRCh38
NC_000001.10:g.197057196_197057200delinsGTTTC , CM000663.1:g.197057196_197057200delinsGTTTC	GRCh37
NC_000001.9:g.195323819_195323823delinsGTTTC	NCBI36
NG_015867.1:g.63625_63629delinsGAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3448+186_3448+190delinsGAAAC
ENST00000367409.9:c.10161+186_10161+190delinsGAAAC MANE Select	ENSP00000356379.4:n.10161+186_10161+190delinsGAAAC
ENST00000680265.1:c.10383+186_10383+190delinsGAAAC	ENSP00000505384.1:n.10383+186_10383+190delinsGAAAC
ENST00000680710.1:c.10137+186_10137+190delinsGAAAC	ENSP00000506676.1:n.10137+186_10137+190delinsGAAAC
ENST00000294732.11:c.5406+186_5406+190delinsGAAAC	ENSP00000294732.7:n.5406+186_5406+190delinsGAAAC
ENST00000367408.5:c.3156+186_3156+190delinsGAAAC	ENSP00000356378.1:n.3156+186_3156+190delinsGAAAC
ENST00000367409.8:c.10161+186_10161+190delinsGAAAC	ENSP00000356379.4:n.10161+186_10161+190delinsGAAAC
NM_001206846.1:c.5406+186_5406+190delinsGAAAC	NP_001193775.1:n.5406+186_5406+190delinsGAAAC
NM_018136.4:c.10161+186_10161+190delinsGAAAC	NP_060606.3:n.10161+186_10161+190delinsGAAAC
NM_018136.5:c.10161+186_10161+190delinsGAAAC MANE Select	NP_060606.3:n.10161+186_10161+190delinsGAAAC
NM_001206846.2:c.5406+186_5406+190delinsGAAAC	NP_001193775.1:n.5406+186_5406+190delinsGAAAC