Canonical Allele Identifier: CA2649660416

Gene: ASPM

Linked Data

• gnomAD v4: 1-197088188-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088191_197088192del , CM000663.2:g.197088191_197088192del	GRCh38
NC_000001.10:g.197057321_197057322del , CM000663.1:g.197057321_197057322del	GRCh37
NC_000001.9:g.195323944_195323945del	NCBI36
NG_015867.1:g.63505_63506del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3448+66_3448+67del
ENST00000367409.9:c.10161+66_10161+67del MANE Select	ENSP00000356379.4:n.10161+66_10161+67del
ENST00000680265.1:c.10383+66_10383+67del	ENSP00000505384.1:n.10383+66_10383+67del
ENST00000680710.1:c.10137+66_10137+67del	ENSP00000506676.1:n.10137+66_10137+67del
ENST00000294732.11:c.5406+66_5406+67del	ENSP00000294732.7:n.5406+66_5406+67del
ENST00000367408.5:c.3156+66_3156+67del	ENSP00000356378.1:n.3156+66_3156+67del
ENST00000367409.8:c.10161+66_10161+67del	ENSP00000356379.4:n.10161+66_10161+67del
NM_001206846.1:c.5406+66_5406+67del	NP_001193775.1:n.5406+66_5406+67del
NM_018136.4:c.10161+66_10161+67del	NP_060606.3:n.10161+66_10161+67del
NM_018136.5:c.10161+66_10161+67del MANE Select	NP_060606.3:n.10161+66_10161+67del
NM_001206846.2:c.5406+66_5406+67del	NP_001193775.1:n.5406+66_5406+67del