Canonical Allele Identifier: CA1217930361

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102618C= , CM000663.2:g.197102618C=	GRCh38
NC_000001.10:g.197071748C= , CM000663.1:g.197071748C=	GRCh37
NC_000001.9:g.195338371C=	NCBI36
NG_015867.1:g.49077G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6454G=
ENST00000367409.9:c.6633G= MANE Select	ENSP00000356379.4:p.Lys2211=
ENST00000680265.1:c.6633G=	ENSP00000505384.1:p.Lys2211=
ENST00000680710.1:c.6633G=	ENSP00000506676.1:p.Lys2211=
ENST00000294732.11:c.4066-6454G=	ENSP00000294732.7:n.4066-6454G=
ENST00000367408.5:c.1816-6454G=	ENSP00000356378.1:n.1816-6454G=
ENST00000367409.8:c.6633G=	ENSP00000356379.4:p.Lys2211=
ENST00000612785.1:c.591G=	ENSP00000479244.1:p.Lys197=
NM_001206846.1:c.4066-6454G=	NP_001193775.1:n.4066-6454G=
NM_018136.4:c.6633G=	NP_060606.3:p.Lys2211=
NM_018136.5:c.6633G= MANE Select	NP_060606.3:p.Lys2211=
NM_001206846.2:c.4066-6454G=	NP_001193775.1:n.4066-6454G=