Canonical Allele Identifier: CA344003353

Gene: ASPM

Linked Data

• gnomAD v4: 1-197090992-T-A
• MyVariant Identifiers: chr1:g.197060122T>A (hg19) ; chr1:g.197090992T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090992T>A , CM000663.2:g.197090992T>A	GRCh38
NC_000001.10:g.197060122T>A , CM000663.1:g.197060122T>A	GRCh37
NC_000001.9:g.195326745T>A	NCBI36
NG_015867.1:g.60703A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2781A>T
ENST00000367409.9:c.9494A>T MANE Select	ENSP00000356379.4:p.His3165Leu
ENST00000680265.1:c.9716A>T	ENSP00000505384.1:p.His3239Leu
ENST00000680710.1:c.9470A>T	ENSP00000506676.1:p.His3157Leu
ENST00000294732.11:c.4739A>T	ENSP00000294732.7:p.His1580Leu
ENST00000367408.5:c.2489A>T	ENSP00000356378.1:p.His830Leu
ENST00000367409.8:c.9494A>T	ENSP00000356379.4:p.His3165Leu
ENST00000612785.1:c.3452A>T	ENSP00000479244.1:p.His1151Leu
NM_001206846.1:c.4739A>T	NP_001193775.1:p.His1580Leu
NM_018136.4:c.9494A>T	NP_060606.3:p.His3165Leu
NM_018136.5:c.9494A>T MANE Select	NP_060606.3:p.His3165Leu
NM_001206846.2:c.4739A>T	NP_001193775.1:p.His1580Leu