Canonical Allele Identifier: CA1309787

Gene: ASPM

Linked Data

• ClinVar Variation Id: 1357652
• ClinVar RCV Id: RCV001894031
• dbSNP Id: rs776605087
• ExAC: 1:197073117 A / G
• gnomAD v2: 1-197073117-A-G
• gnomAD v3: 1-197103987-A-G
• gnomAD v4: 1-197103987-A-G
• MyVariant Identifiers: chr1:g.197073117A>G (hg19) ; chr1:g.197103987A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103987A>G , CM000663.2:g.197103987A>G	GRCh38
NC_000001.10:g.197073117A>G , CM000663.1:g.197073117A>G	GRCh37
NC_000001.9:g.195339740A>G	NCBI36
NG_015867.1:g.47708T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7823T>C
ENST00000367409.9:c.5264T>C MANE Select	ENSP00000356379.4:p.Val1755Ala
ENST00000680265.1:c.5264T>C	ENSP00000505384.1:p.Val1755Ala
ENST00000680710.1:c.5264T>C	ENSP00000506676.1:p.Val1755Ala
ENST00000294732.11:c.4066-7823T>C	ENSP00000294732.7:n.4066-7823T>C
ENST00000367408.5:c.1816-7823T>C	ENSP00000356378.1:n.1816-7823T>C
ENST00000367409.8:c.5264T>C	ENSP00000356379.4:p.Val1755Ala
ENST00000612785.1:c.562-1340T>C	ENSP00000479244.1:n.562-1340T>C
NM_001206846.1:c.4066-7823T>C	NP_001193775.1:n.4066-7823T>C
NM_018136.4:c.5264T>C	NP_060606.3:p.Val1755Ala
NM_018136.5:c.5264T>C MANE Select	NP_060606.3:p.Val1755Ala
NM_001206846.2:c.4066-7823T>C	NP_001193775.1:n.4066-7823T>C