Canonical Allele Identifier: CA1217923552

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088348G= , CM000663.2:g.197088348G=	GRCh38
NC_000001.10:g.197057478G= , CM000663.1:g.197057478G=	GRCh37
NC_000001.9:g.195324101G=	NCBI36
NG_015867.1:g.63347C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3356C=
ENST00000367409.9:c.10069C= MANE Select	ENSP00000356379.4:p.Pro3357=
ENST00000680265.1:c.10291C=	ENSP00000505384.1:p.Pro3431=
ENST00000680710.1:c.10045C=	ENSP00000506676.1:p.Pro3349=
ENST00000294732.11:c.5314C=	ENSP00000294732.7:p.Pro1772=
ENST00000367408.5:c.3064C=	ENSP00000356378.1:p.Pro1022=
ENST00000367409.8:c.10069C=	ENSP00000356379.4:p.Pro3357=
ENST00000612785.1:c.4027C=	ENSP00000479244.1:p.Pro1343=
NM_001206846.1:c.5314C=	NP_001193775.1:p.Pro1772=
NM_018136.4:c.10069C=	NP_060606.3:p.Pro3357=
NM_018136.5:c.10069C= MANE Select	NP_060606.3:p.Pro3357=
NM_001206846.2:c.5314C=	NP_001193775.1:p.Pro1772=