Canonical Allele Identifier: CA343998557

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057516T>A (hg19) ; chr1:g.197088386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088386T>A , CM000663.2:g.197088386T>A	GRCh38
NC_000001.10:g.197057516T>A , CM000663.1:g.197057516T>A	GRCh37
NC_000001.9:g.195324139T>A	NCBI36
NG_015867.1:g.63309A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3318A>T
ENST00000367409.9:c.10031A>T MANE Select	ENSP00000356379.4:p.Asp3344Val
ENST00000680265.1:c.10253A>T	ENSP00000505384.1:p.Asp3418Val
ENST00000680710.1:c.10007A>T	ENSP00000506676.1:p.Asp3336Val
ENST00000294732.11:c.5276A>T	ENSP00000294732.7:p.Asp1759Val
ENST00000367408.5:c.3026A>T	ENSP00000356378.1:p.Asp1009Val
ENST00000367409.8:c.10031A>T	ENSP00000356379.4:p.Asp3344Val
ENST00000612785.1:c.3989A>T	ENSP00000479244.1:p.Asp1330Val
NM_001206846.1:c.5276A>T	NP_001193775.1:p.Asp1759Val
NM_018136.4:c.10031A>T	NP_060606.3:p.Asp3344Val
NM_018136.5:c.10031A>T MANE Select	NP_060606.3:p.Asp3344Val
NM_001206846.2:c.5276A>T	NP_001193775.1:p.Asp1759Val