Canonical Allele Identifier: CA1217926732

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093233G= , CM000663.2:g.197093233G=	GRCh38
NC_000001.10:g.197062363G= , CM000663.1:g.197062363G=	GRCh37
NC_000001.9:g.195328986G=	NCBI36
NG_015867.1:g.58462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2400C=
ENST00000367409.9:c.9113C= MANE Select	ENSP00000356379.4:p.Ala3038=
ENST00000680265.1:c.9335C=	ENSP00000505384.1:p.Ala3112=
ENST00000680710.1:c.9113C=	ENSP00000506676.1:p.Ala3038=
ENST00000294732.11:c.4358C=	ENSP00000294732.7:p.Ala1453=
ENST00000367408.5:c.2108C=	ENSP00000356378.1:p.Ala703=
ENST00000367409.8:c.9113C=	ENSP00000356379.4:p.Ala3038=
ENST00000612785.1:c.3071C=	ENSP00000479244.1:p.Ala1024=
NM_001206846.1:c.4358C=	NP_001193775.1:p.Ala1453=
NM_018136.4:c.9113C=	NP_060606.3:p.Ala3038=
NM_018136.5:c.9113C= MANE Select	NP_060606.3:p.Ala3038=
NM_001206846.2:c.4358C=	NP_001193775.1:p.Ala1453=