Canonical Allele Identifier: CA344036384

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197087006C>A (hg19) ; chr1:g.197117876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117876C>A , CM000663.2:g.197117876C>A	GRCh38
NC_000001.10:g.197087006C>A , CM000663.1:g.197087006C>A	GRCh37
NC_000001.9:g.195353629C>A	NCBI36
NG_015867.1:g.33819G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2020G>T
ENST00000367409.9:c.3978G>T MANE Select	ENSP00000356379.4:p.Trp1326Cys
ENST00000680265.1:c.3978G>T	ENSP00000505384.1:p.Trp1326Cys
ENST00000680710.1:c.3978G>T	ENSP00000506676.1:p.Trp1326Cys
ENST00000681879.1:c.4026G>T	ENSP00000505363.1:n.4026G>T
ENST00000294732.11:c.3978G>T	ENSP00000294732.7:p.Trp1326Cys
ENST00000367408.5:c.1728G>T	ENSP00000356378.1:p.Trp576Cys
ENST00000367409.8:c.3978G>T	ENSP00000356379.4:p.Trp1326Cys
ENST00000612785.1:c.562-15229G>T	ENSP00000479244.1:n.562-15229G>T
NM_001206846.1:c.3978G>T	NP_001193775.1:p.Trp1326Cys
NM_018136.4:c.3978G>T	NP_060606.3:p.Trp1326Cys
NM_018136.5:c.3978G>T MANE Select	NP_060606.3:p.Trp1326Cys
NM_001206846.2:c.3978G>T	NP_001193775.1:p.Trp1326Cys