Canonical Allele Identifier: CA1217930761

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103651G= , CM000663.2:g.197103651G=	GRCh38
NC_000001.10:g.197072781G= , CM000663.1:g.197072781G=	GRCh37
NC_000001.9:g.195339404G=	NCBI36
NG_015867.1:g.48044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7487C=
ENST00000367409.9:c.5600C= MANE Select	ENSP00000356379.4:p.Thr1867=
ENST00000680265.1:c.5600C=	ENSP00000505384.1:p.Thr1867=
ENST00000680710.1:c.5600C=	ENSP00000506676.1:p.Thr1867=
ENST00000294732.11:c.4066-7487C=	ENSP00000294732.7:n.4066-7487C=
ENST00000367408.5:c.1816-7487C=	ENSP00000356378.1:n.1816-7487C=
ENST00000367409.8:c.5600C=	ENSP00000356379.4:p.Thr1867=
ENST00000612785.1:c.562-1004C=	ENSP00000479244.1:n.562-1004C=
NM_001206846.1:c.4066-7487C=	NP_001193775.1:n.4066-7487C=
NM_018136.4:c.5600C=	NP_060606.3:p.Thr1867=
NM_018136.5:c.5600C= MANE Select	NP_060606.3:p.Thr1867=
NM_001206846.2:c.4066-7487C=	NP_001193775.1:n.4066-7487C=