Canonical Allele Identifier: CA1149061114

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088327T= , CM000663.2:g.197088327T=	GRCh38
NC_000001.10:g.197057457T= , CM000663.1:g.197057457T=	GRCh37
NC_000001.9:g.195324080T=	NCBI36
NG_015867.1:g.63368A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3377A=
ENST00000367409.9:c.10090A= MANE Select	ENSP00000356379.4:p.Lys3364=
ENST00000680265.1:c.10312A=	ENSP00000505384.1:p.Lys3438=
ENST00000680710.1:c.10066A=	ENSP00000506676.1:p.Lys3356=
ENST00000294732.11:c.5335A=	ENSP00000294732.7:p.Lys1779=
ENST00000367408.5:c.3085A=	ENSP00000356378.1:p.Lys1029=
ENST00000367409.8:c.10090A=	ENSP00000356379.4:p.Lys3364=
ENST00000612785.1:c.4048A=	ENSP00000479244.1:p.Lys1350=
NM_001206846.1:c.5335A=	NP_001193775.1:p.Lys1779=
NM_018136.4:c.10090A=	NP_060606.3:p.Lys3364=
NM_018136.5:c.10090A= MANE Select	NP_060606.3:p.Lys3364=
NM_001206846.2:c.5335A=	NP_001193775.1:p.Lys1779=