Canonical Allele Identifier: CA344014345

Gene: ASPM

Linked Data

• ClinVar Variation Id: 2072751
• ClinVar RCV Id: RCV002949641
• MyVariant Identifiers: chr1:g.197070379C>T (hg19) ; chr1:g.197101249C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101249C>T , CM000663.2:g.197101249C>T	GRCh38
NC_000001.10:g.197070379C>T , CM000663.1:g.197070379C>T	GRCh37
NC_000001.9:g.195337002C>T	NCBI36
NG_015867.1:g.50446G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-5085G>A
ENST00000367409.9:c.8002G>A MANE Select	ENSP00000356379.4:p.Ala2668Thr
ENST00000680265.1:c.8002G>A	ENSP00000505384.1:p.Ala2668Thr
ENST00000680710.1:c.8002G>A	ENSP00000506676.1:p.Ala2668Thr
ENST00000294732.11:c.4066-5085G>A	ENSP00000294732.7:n.4066-5085G>A
ENST00000367408.5:c.1816-5085G>A	ENSP00000356378.1:n.1816-5085G>A
ENST00000367409.8:c.8002G>A	ENSP00000356379.4:p.Ala2668Thr
ENST00000612785.1:c.1960G>A	ENSP00000479244.1:p.Ala654Thr
NM_001206846.1:c.4066-5085G>A	NP_001193775.1:n.4066-5085G>A
NM_018136.4:c.8002G>A	NP_060606.3:p.Ala2668Thr
NM_018136.5:c.8002G>A MANE Select	NP_060606.3:p.Ala2668Thr
NM_001206846.2:c.4066-5085G>A	NP_001193775.1:n.4066-5085G>A