Canonical Allele Identifier: CA344022863

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197071926G>T (hg19) ; chr1:g.197102796G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102796G>T , CM000663.2:g.197102796G>T	GRCh38
NC_000001.10:g.197071926G>T , CM000663.1:g.197071926G>T	GRCh37
NC_000001.9:g.195338549G>T	NCBI36
NG_015867.1:g.48899C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6632C>A
ENST00000367409.9:c.6455C>A MANE Select	ENSP00000356379.4:p.Ala2152Glu
ENST00000680265.1:c.6455C>A	ENSP00000505384.1:p.Ala2152Glu
ENST00000680710.1:c.6455C>A	ENSP00000506676.1:p.Ala2152Glu
ENST00000294732.11:c.4066-6632C>A	ENSP00000294732.7:n.4066-6632C>A
ENST00000367408.5:c.1816-6632C>A	ENSP00000356378.1:n.1816-6632C>A
ENST00000367409.8:c.6455C>A	ENSP00000356379.4:p.Ala2152Glu
ENST00000612785.1:c.562-149C>A	ENSP00000479244.1:n.562-149C>A
NM_001206846.1:c.4066-6632C>A	NP_001193775.1:n.4066-6632C>A
NM_018136.4:c.6455C>A	NP_060606.3:p.Ala2152Glu
NM_018136.5:c.6455C>A MANE Select	NP_060606.3:p.Ala2152Glu
NM_001206846.2:c.4066-6632C>A	NP_001193775.1:n.4066-6632C>A