Canonical Allele Identifier: CA343998850

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057562A>C (hg19) ; chr1:g.197088432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088432A>C , CM000663.2:g.197088432A>C	GRCh38
NC_000001.10:g.197057562A>C , CM000663.1:g.197057562A>C	GRCh37
NC_000001.9:g.195324185A>C	NCBI36
NG_015867.1:g.63263T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3272T>G
ENST00000367409.9:c.9985T>G MANE Select	ENSP00000356379.4:p.Tyr3329Asp
ENST00000680265.1:c.10207T>G	ENSP00000505384.1:p.Tyr3403Asp
ENST00000680710.1:c.9961T>G	ENSP00000506676.1:p.Tyr3321Asp
ENST00000294732.11:c.5230T>G	ENSP00000294732.7:p.Tyr1744Asp
ENST00000367408.5:c.2980T>G	ENSP00000356378.1:p.Tyr994Asp
ENST00000367409.8:c.9985T>G	ENSP00000356379.4:p.Tyr3329Asp
ENST00000612785.1:c.3943T>G	ENSP00000479244.1:p.Tyr1315Asp
NM_001206846.1:c.5230T>G	NP_001193775.1:p.Tyr1744Asp
NM_018136.4:c.9985T>G	NP_060606.3:p.Tyr3329Asp
NM_018136.5:c.9985T>G MANE Select	NP_060606.3:p.Tyr3329Asp
NM_001206846.2:c.5230T>G	NP_001193775.1:p.Tyr1744Asp