Canonical Allele Identifier: CA344003015

Gene: ASPM

Linked Data

• COSMIC: COSM678355
• MyVariant Identifiers: chr1:g.197060090C>G (hg19) ; chr1:g.197090960C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2813G>C
ENST00000367409.9:c.9526G>C MANE Select	ENSP00000356379.4:p.Glu3176Gln
ENST00000680265.1:c.9748G>C	ENSP00000505384.1:p.Glu3250Gln
ENST00000680710.1:c.9502G>C	ENSP00000506676.1:p.Glu3168Gln
ENST00000294732.11:c.4771G>C	ENSP00000294732.7:p.Glu1591Gln
ENST00000367408.5:c.2521G>C	ENSP00000356378.1:p.Glu841Gln
ENST00000367409.8:c.9526G>C	ENSP00000356379.4:p.Glu3176Gln
ENST00000612785.1:c.3484G>C	ENSP00000479244.1:p.Glu1162Gln
NM_001206846.1:c.4771G>C	NP_001193775.1:p.Glu1591Gln
NM_018136.4:c.9526G>C	NP_060606.3:p.Glu3176Gln
NM_018136.5:c.9526G>C MANE Select	NP_060606.3:p.Glu3176Gln
NM_001206846.2:c.4771G>C	NP_001193775.1:p.Glu1591Gln