Canonical Allele Identifier: CA344003012

Gene: ASPM

Linked Data

• COSMIC: COSM5636226
• MyVariant Identifiers: chr1:g.197060090C>T (hg19) ; chr1:g.197090960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090960C>T , CM000663.2:g.197090960C>T	GRCh38
NC_000001.10:g.197060090C>T , CM000663.1:g.197060090C>T	GRCh37
NC_000001.9:g.195326713C>T	NCBI36
NG_015867.1:g.60735G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2813G>A
ENST00000367409.9:c.9526G>A MANE Select	ENSP00000356379.4:p.Glu3176Lys
ENST00000680265.1:c.9748G>A	ENSP00000505384.1:p.Glu3250Lys
ENST00000680710.1:c.9502G>A	ENSP00000506676.1:p.Glu3168Lys
ENST00000294732.11:c.4771G>A	ENSP00000294732.7:p.Glu1591Lys
ENST00000367408.5:c.2521G>A	ENSP00000356378.1:p.Glu841Lys
ENST00000367409.8:c.9526G>A	ENSP00000356379.4:p.Glu3176Lys
ENST00000612785.1:c.3484G>A	ENSP00000479244.1:p.Glu1162Lys
NM_001206846.1:c.4771G>A	NP_001193775.1:p.Glu1591Lys
NM_018136.4:c.9526G>A	NP_060606.3:p.Glu3176Lys
NM_018136.5:c.9526G>A MANE Select	NP_060606.3:p.Glu3176Lys
NM_001206846.2:c.4771G>A	NP_001193775.1:p.Glu1591Lys