Canonical Allele Identifier: CA1217938398

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197121846C= , CM000663.2:g.197121846C=	GRCh38
NC_000001.10:g.197090976C= , CM000663.1:g.197090976C=	GRCh37
NC_000001.9:g.195357599C=	NCBI36
NG_015867.1:g.29849G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1912+69G=
ENST00000367409.9:c.3870+69G= MANE Select	ENSP00000356379.4:n.3870+69G=
ENST00000680112.1:n.1995G=
ENST00000680265.1:c.3870+69G=	ENSP00000505384.1:n.3870+69G=
ENST00000680710.1:c.3870+69G=	ENSP00000506676.1:n.3870+69G=
ENST00000681879.1:c.3918+21G=	ENSP00000505363.1:n.3918+21G=
ENST00000294732.11:c.3870+69G=	ENSP00000294732.7:n.3870+69G=
ENST00000367408.5:c.1620+69G=	ENSP00000356378.1:n.1620+69G=
ENST00000367409.8:c.3870+69G=	ENSP00000356379.4:n.3870+69G=
ENST00000612785.1:c.562-19199G=	ENSP00000479244.1:n.562-19199G=
NM_001206846.1:c.3870+69G=	NP_001193775.1:n.3870+69G=
NM_018136.4:c.3870+69G=	NP_060606.3:n.3870+69G=
NM_018136.5:c.3870+69G= MANE Select	NP_060606.3:n.3870+69G=
NM_001206846.2:c.3870+69G=	NP_001193775.1:n.3870+69G=