Canonical Allele Identifier: CA1144152795

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088257G= , CM000663.2:g.197088257G=	GRCh38
NC_000001.10:g.197057387G= , CM000663.1:g.197057387G=	GRCh37
NC_000001.9:g.195324010G=	NCBI36
NG_015867.1:g.63438C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3447C=
ENST00000367409.9:c.10160C= MANE Select	ENSP00000356379.4:p.Ser3387=
ENST00000680265.1:c.10382C=	ENSP00000505384.1:p.Ser3461=
ENST00000680710.1:c.10136C=	ENSP00000506676.1:p.Ser3379=
ENST00000294732.11:c.5405C=	ENSP00000294732.7:p.Ser1802=
ENST00000367408.5:c.3155C=	ENSP00000356378.1:p.Ser1052=
ENST00000367409.8:c.10160C=	ENSP00000356379.4:p.Ser3387=
ENST00000612785.1:c.4118C=	ENSP00000479244.1:p.Ser1373=
NM_001206846.1:c.5405C=	NP_001193775.1:p.Ser1802=
NM_018136.4:c.10160C=	NP_060606.3:p.Ser3387=
NM_018136.5:c.10160C= MANE Select	NP_060606.3:p.Ser3387=
NM_001206846.2:c.5405C=	NP_001193775.1:p.Ser1802=