Canonical Allele Identifier: CA2649660663

Gene: ASPM

Linked Data

• gnomAD v4: 1-197090430-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090430T>A , CM000663.2:g.197090430T>A	GRCh38
NC_000001.10:g.197059560T>A , CM000663.1:g.197059560T>A	GRCh37
NC_000001.9:g.195326183T>A	NCBI36
NG_015867.1:g.61265A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2924-42A>T
ENST00000367409.9:c.9637-42A>T MANE Select	ENSP00000356379.4:n.9637-42A>T
ENST00000680265.1:c.9859-42A>T	ENSP00000505384.1:n.9859-42A>T
ENST00000680710.1:c.9613-42A>T	ENSP00000506676.1:n.9613-42A>T
ENST00000294732.11:c.4882-42A>T	ENSP00000294732.7:n.4882-42A>T
ENST00000367408.5:c.2632-42A>T	ENSP00000356378.1:n.2632-42A>T
ENST00000367409.8:c.9637-42A>T	ENSP00000356379.4:n.9637-42A>T
ENST00000612785.1:c.3595-42A>T	ENSP00000479244.1:n.3595-42A>T
NM_001206846.1:c.4882-42A>T	NP_001193775.1:n.4882-42A>T
NM_018136.4:c.9637-42A>T	NP_060606.3:n.9637-42A>T
NM_018136.5:c.9637-42A>T MANE Select	NP_060606.3:n.9637-42A>T
NM_001206846.2:c.4882-42A>T	NP_001193775.1:n.4882-42A>T