Canonical Allele Identifier: CA1148878277

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090350A= , CM000663.2:g.197090350A=	GRCh38
NC_000001.10:g.197059480A= , CM000663.1:g.197059480A=	GRCh37
NC_000001.9:g.195326103A=	NCBI36
NG_015867.1:g.61345T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2962T=
ENST00000367409.9:c.9675T= MANE Select	ENSP00000356379.4:p.Asp3225=
ENST00000680265.1:c.9897T=	ENSP00000505384.1:p.Asp3299=
ENST00000680710.1:c.9651T=	ENSP00000506676.1:p.Asp3217=
ENST00000294732.11:c.4920T=	ENSP00000294732.7:p.Asp1640=
ENST00000367408.5:c.2670T=	ENSP00000356378.1:p.Asp890=
ENST00000367409.8:c.9675T=	ENSP00000356379.4:p.Asp3225=
ENST00000612785.1:c.3633T=	ENSP00000479244.1:p.Asp1211=
NM_001206846.1:c.4920T=	NP_001193775.1:p.Asp1640=
NM_018136.4:c.9675T=	NP_060606.3:p.Asp3225=
NM_018136.5:c.9675T= MANE Select	NP_060606.3:p.Asp3225=
NM_001206846.2:c.4920T=	NP_001193775.1:p.Asp1640=