Canonical Allele Identifier: CA422805345

Gene: ASPM

Linked Data

• ClinVar Variation Id: 2802201
• ClinVar RCV Id: RCV003668701
• dbSNP Id: rs777899411
• gnomAD v2: 1-197069756-G-C
• gnomAD v4: 1-197100626-G-C
• MyVariant Identifiers: chr1:g.197069756G>C (hg19) ; chr1:g.197100626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197100626G>C , CM000663.2:g.197100626G>C	GRCh38
NC_000001.10:g.197069756G>C , CM000663.1:g.197069756G>C	GRCh37
NC_000001.9:g.195336379G>C	NCBI36
NG_015867.1:g.51069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-4462C>G
ENST00000367409.9:c.8625C>G MANE Select	ENSP00000356379.4:p.Thr2875=
ENST00000680265.1:c.8625C>G	ENSP00000505384.1:p.Thr2875=
ENST00000680710.1:c.8625C>G	ENSP00000506676.1:p.Thr2875=
ENST00000294732.11:c.4066-4462C>G	ENSP00000294732.7:n.4066-4462C>G
ENST00000367408.5:c.1816-4462C>G	ENSP00000356378.1:n.1816-4462C>G
ENST00000367409.8:c.8625C>G	ENSP00000356379.4:p.Thr2875=
ENST00000612785.1:c.2583C>G	ENSP00000479244.1:p.Thr861=
NM_001206846.1:c.4066-4462C>G	NP_001193775.1:n.4066-4462C>G
NM_018136.4:c.8625C>G	NP_060606.3:p.Thr2875=
NM_018136.5:c.8625C>G MANE Select	NP_060606.3:p.Thr2875=
NM_001206846.2:c.4066-4462C>G	NP_001193775.1:n.4066-4462C>G