Canonical Allele Identifier: CA35861098

Gene: ASPM

Linked Data

• dbSNP Id: rs1027210183
• gnomAD v4: 1-197088388-T-C
• MyVariant Identifiers: chr1:g.197057518T>C (hg19) ; chr1:g.197088388T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088388T>C , CM000663.2:g.197088388T>C	GRCh38
NC_000001.10:g.197057518T>C , CM000663.1:g.197057518T>C	GRCh37
NC_000001.9:g.195324141T>C	NCBI36
NG_015867.1:g.63307A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3316A>G
ENST00000367409.9:c.10029A>G MANE Select	ENSP00000356379.4:p.Ile3343Met
ENST00000680265.1:c.10251A>G	ENSP00000505384.1:p.Ile3417Met
ENST00000680710.1:c.10005A>G	ENSP00000506676.1:p.Ile3335Met
ENST00000294732.11:c.5274A>G	ENSP00000294732.7:p.Ile1758Met
ENST00000367408.5:c.3024A>G	ENSP00000356378.1:p.Ile1008Met
ENST00000367409.8:c.10029A>G	ENSP00000356379.4:p.Ile3343Met
ENST00000612785.1:c.3987A>G	ENSP00000479244.1:p.Ile1329Met
NM_001206846.1:c.5274A>G	NP_001193775.1:p.Ile1758Met
NM_018136.4:c.10029A>G	NP_060606.3:p.Ile3343Met
NM_018136.5:c.10029A>G MANE Select	NP_060606.3:p.Ile3343Met
NM_001206846.2:c.5274A>G	NP_001193775.1:p.Ile1758Met