Canonical Allele Identifier: CA1217925064

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090132A= , CM000663.2:g.197090132A=	GRCh38
NC_000001.10:g.197059262A= , CM000663.1:g.197059262A=	GRCh37
NC_000001.9:g.195325885A=	NCBI36
NG_015867.1:g.61563T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3117-48T=
ENST00000367409.9:c.9830-48T= MANE Select	ENSP00000356379.4:n.9830-48T=
ENST00000680265.1:c.10052-48T=	ENSP00000505384.1:n.10052-48T=
ENST00000680710.1:c.9806-48T=	ENSP00000506676.1:n.9806-48T=
ENST00000294732.11:c.5075-48T=	ENSP00000294732.7:n.5075-48T=
ENST00000367408.5:c.2825-48T=	ENSP00000356378.1:n.2825-48T=
ENST00000367409.8:c.9830-48T=	ENSP00000356379.4:n.9830-48T=
ENST00000612785.1:c.3788-48T=	ENSP00000479244.1:n.3788-48T=
NM_001206846.1:c.5075-48T=	NP_001193775.1:n.5075-48T=
NM_018136.4:c.9830-48T=	NP_060606.3:n.9830-48T=
NM_018136.5:c.9830-48T= MANE Select	NP_060606.3:n.9830-48T=
NM_001206846.2:c.5075-48T=	NP_001193775.1:n.5075-48T=