Canonical Allele Identifier: CA344007163

Gene: ASPM

Linked Data

• dbSNP Id: rs1406859691
• gnomAD v4: 1-197093159-T-A
• MyVariant Identifiers: chr1:g.197062289T>A (hg19) ; chr1:g.197093159T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093159T>A , CM000663.2:g.197093159T>A	GRCh38
NC_000001.10:g.197062289T>A , CM000663.1:g.197062289T>A	GRCh37
NC_000001.9:g.195328912T>A	NCBI36
NG_015867.1:g.58536A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2474A>T
ENST00000367409.9:c.9187A>T MANE Select	ENSP00000356379.4:p.Ile3063Leu
ENST00000680265.1:c.9409A>T	ENSP00000505384.1:p.Ile3137Leu
ENST00000680710.1:c.9187A>T	ENSP00000506676.1:p.Ile3063Leu
ENST00000294732.11:c.4432A>T	ENSP00000294732.7:p.Ile1478Leu
ENST00000367408.5:c.2182A>T	ENSP00000356378.1:p.Ile728Leu
ENST00000367409.8:c.9187A>T	ENSP00000356379.4:p.Ile3063Leu
ENST00000612785.1:c.3145A>T	ENSP00000479244.1:p.Ile1049Leu
NM_001206846.1:c.4432A>T	NP_001193775.1:p.Ile1478Leu
NM_018136.4:c.9187A>T	NP_060606.3:p.Ile3063Leu
NM_018136.5:c.9187A>T MANE Select	NP_060606.3:p.Ile3063Leu
NM_001206846.2:c.4432A>T	NP_001193775.1:p.Ile1478Leu