Canonical Allele Identifier: CA344001682

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059361T>C (hg19) ; chr1:g.197090231T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090231T>C , CM000663.2:g.197090231T>C	GRCh38
NC_000001.10:g.197059361T>C , CM000663.1:g.197059361T>C	GRCh37
NC_000001.9:g.195325984T>C	NCBI36
NG_015867.1:g.61464A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3081A>G
ENST00000367409.9:c.9794A>G MANE Select	ENSP00000356379.4:p.His3265Arg
ENST00000680265.1:c.10016A>G	ENSP00000505384.1:p.His3339Arg
ENST00000680710.1:c.9770A>G	ENSP00000506676.1:p.His3257Arg
ENST00000294732.11:c.5039A>G	ENSP00000294732.7:p.His1680Arg
ENST00000367408.5:c.2789A>G	ENSP00000356378.1:p.His930Arg
ENST00000367409.8:c.9794A>G	ENSP00000356379.4:p.His3265Arg
ENST00000612785.1:c.3752A>G	ENSP00000479244.1:p.His1251Arg
NM_001206846.1:c.5039A>G	NP_001193775.1:p.His1680Arg
NM_018136.4:c.9794A>G	NP_060606.3:p.His3265Arg
NM_018136.5:c.9794A>G MANE Select	NP_060606.3:p.His3265Arg
NM_001206846.2:c.5039A>G	NP_001193775.1:p.His1680Arg