Canonical Allele Identifier: CA1217938561

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122350A= , CM000663.2:g.197122350A=	GRCh38
NC_000001.10:g.197091480A= , CM000663.1:g.197091480A=	GRCh37
NC_000001.9:g.195358103A=	NCBI36
NG_015867.1:g.29345T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1640+38T=
ENST00000367409.9:c.3598+38T= MANE Select	ENSP00000356379.4:n.3598+38T=
ENST00000680112.1:n.1654+38T=
ENST00000680265.1:c.3598+38T=	ENSP00000505384.1:n.3598+38T=
ENST00000680710.1:c.3598+38T=	ENSP00000506676.1:n.3598+38T=
ENST00000681879.1:c.3598+38T=	ENSP00000505363.1:n.3598+38T=
ENST00000294732.11:c.3598+38T=	ENSP00000294732.7:n.3598+38T=
ENST00000367408.5:c.1348+38T=	ENSP00000356378.1:n.1348+38T=
ENST00000367409.8:c.3598+38T=	ENSP00000356379.4:n.3598+38T=
ENST00000612785.1:c.562-19703T=	ENSP00000479244.1:n.562-19703T=
NM_001206846.1:c.3598+38T=	NP_001193775.1:n.3598+38T=
NM_018136.4:c.3598+38T=	NP_060606.3:n.3598+38T=
NM_018136.5:c.3598+38T= MANE Select	NP_060606.3:n.3598+38T=
NM_001206846.2:c.3598+38T=	NP_001193775.1:n.3598+38T=