Canonical Allele Identifier: CA343998032

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057465A>T (hg19) ; chr1:g.197088335A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088335A>T , CM000663.2:g.197088335A>T	GRCh38
NC_000001.10:g.197057465A>T , CM000663.1:g.197057465A>T	GRCh37
NC_000001.9:g.195324088A>T	NCBI36
NG_015867.1:g.63360T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3369T>A
ENST00000367409.9:c.10082T>A MANE Select	ENSP00000356379.4:p.Val3361Asp
ENST00000680265.1:c.10304T>A	ENSP00000505384.1:p.Val3435Asp
ENST00000680710.1:c.10058T>A	ENSP00000506676.1:p.Val3353Asp
ENST00000294732.11:c.5327T>A	ENSP00000294732.7:p.Val1776Asp
ENST00000367408.5:c.3077T>A	ENSP00000356378.1:p.Val1026Asp
ENST00000367409.8:c.10082T>A	ENSP00000356379.4:p.Val3361Asp
ENST00000612785.1:c.4040T>A	ENSP00000479244.1:p.Val1347Asp
NM_001206846.1:c.5327T>A	NP_001193775.1:p.Val1776Asp
NM_018136.4:c.10082T>A	NP_060606.3:p.Val3361Asp
NM_018136.5:c.10082T>A MANE Select	NP_060606.3:p.Val3361Asp
NM_001206846.2:c.5327T>A	NP_001193775.1:p.Val1776Asp