Canonical Allele Identifier: CA2649660425

Gene: ASPM

Linked Data

• gnomAD v4: 1-197088221-ATAATCTTAAAGAAAGGCAACTGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088226_197088249del , CM000663.2:g.197088226_197088249del	GRCh38
NC_000001.10:g.197057356_197057379del , CM000663.1:g.197057356_197057379del	GRCh37
NC_000001.9:g.195323979_195324002del	NCBI36
NG_015867.1:g.63450_63473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3448+11_3448+34del
ENST00000367409.9:c.10161+11_10161+34del MANE Select	ENSP00000356379.4:n.10161+11_10161+34del
ENST00000680265.1:c.10383+11_10383+34del	ENSP00000505384.1:n.10383+11_10383+34del
ENST00000680710.1:c.10137+11_10137+34del	ENSP00000506676.1:n.10137+11_10137+34del
ENST00000294732.11:c.5406+11_5406+34del	ENSP00000294732.7:n.5406+11_5406+34del
ENST00000367408.5:c.3156+11_3156+34del	ENSP00000356378.1:n.3156+11_3156+34del
ENST00000367409.8:c.10161+11_10161+34del	ENSP00000356379.4:n.10161+11_10161+34del
ENST00000612785.1:c.4130_4153del	ENSP00000479244.1:p.Ser1377_Ile1384del
NM_001206846.1:c.5406+11_5406+34del	NP_001193775.1:n.5406+11_5406+34del
NM_018136.4:c.10161+11_10161+34del	NP_060606.3:n.10161+11_10161+34del
NM_018136.5:c.10161+11_10161+34del MANE Select	NP_060606.3:n.10161+11_10161+34del
NM_001206846.2:c.5406+11_5406+34del	NP_001193775.1:n.5406+11_5406+34del