Canonical Allele Identifier: CA2649664213

Gene: ASPM

Linked Data

• gnomAD v4: 1-197142865-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142869_197142871del , CM000663.2:g.197142869_197142871del	GRCh38
NC_000001.10:g.197111999_197112001del , CM000663.1:g.197111999_197112001del	GRCh37
NC_000001.9:g.195378622_195378624del	NCBI36
NG_015867.1:g.8827_8829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1384_1386del MANE Select	ENSP00000356379.4:p.Tyr462del
ENST00000679766.1:n.1601_1603del
ENST00000680265.1:c.1384_1386del	ENSP00000505384.1:p.Tyr462del
ENST00000680710.1:c.1384_1386del	ENSP00000506676.1:p.Tyr462del
ENST00000681879.1:c.1384_1386del	ENSP00000505363.1:p.Tyr462del
ENST00000294732.11:c.1384_1386del	ENSP00000294732.7:p.Tyr462del
ENST00000367409.8:c.1384_1386del	ENSP00000356379.4:p.Tyr462del
ENST00000612785.1:c.561+823_561+825del	ENSP00000479244.1:n.561+823_561+825del
NM_001206846.1:c.1384_1386del	NP_001193775.1:p.Tyr462del
NM_018136.4:c.1384_1386del	NP_060606.3:p.Tyr462del
NM_018136.5:c.1384_1386del MANE Select	NP_060606.3:p.Tyr462del
NM_001206846.2:c.1384_1386del	NP_001193775.1:p.Tyr462del