Canonical Allele Identifier: CA344014966

Gene: ASPM

Linked Data

• ClinVar Variation Id: 1379010
• ClinVar RCV Id: RCV001891884
• dbSNP Id: rs1386556330
• MyVariant Identifiers: chr1:g.197111710A>C (hg19) ; chr1:g.197142580A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142580A>C , CM000663.2:g.197142580A>C	GRCh38
NC_000001.10:g.197111710A>C , CM000663.1:g.197111710A>C	GRCh37
NC_000001.9:g.195378333A>C	NCBI36
NG_015867.1:g.9115T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367409.9:c.1672T>G MANE Select	ENSP00000356379.4:p.Tyr558Asp
ENST00000679766.1:n.1889T>G
ENST00000680265.1:c.1672T>G	ENSP00000505384.1:p.Tyr558Asp
ENST00000680710.1:c.1672T>G	ENSP00000506676.1:p.Tyr558Asp
ENST00000681879.1:c.1672T>G	ENSP00000505363.1:p.Tyr558Asp
ENST00000294732.11:c.1672T>G	ENSP00000294732.7:p.Tyr558Asp
ENST00000367409.8:c.1672T>G	ENSP00000356379.4:p.Tyr558Asp
ENST00000612785.1:c.561+1111T>G	ENSP00000479244.1:n.561+1111T>G
NM_001206846.1:c.1672T>G	NP_001193775.1:p.Tyr558Asp
NM_018136.4:c.1672T>G	NP_060606.3:p.Tyr558Asp
NM_018136.5:c.1672T>G MANE Select	NP_060606.3:p.Tyr558Asp
NM_001206846.2:c.1672T>G	NP_001193775.1:p.Tyr558Asp