Canonical Allele Identifier: CA1217923516

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088310A= , CM000663.2:g.197088310A=	GRCh38
NC_000001.10:g.197057440A= , CM000663.1:g.197057440A=	GRCh37
NC_000001.9:g.195324063A=	NCBI36
NG_015867.1:g.63385T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3394T=
ENST00000367409.9:c.10107T= MANE Select	ENSP00000356379.4:p.Phe3369=
ENST00000680265.1:c.10329T=	ENSP00000505384.1:p.Phe3443=
ENST00000680710.1:c.10083T=	ENSP00000506676.1:p.Phe3361=
ENST00000294732.11:c.5352T=	ENSP00000294732.7:p.Phe1784=
ENST00000367408.5:c.3102T=	ENSP00000356378.1:p.Phe1034=
ENST00000367409.8:c.10107T=	ENSP00000356379.4:p.Phe3369=
ENST00000612785.1:c.4065T=	ENSP00000479244.1:p.Phe1355=
NM_001206846.1:c.5352T=	NP_001193775.1:p.Phe1784=
NM_018136.4:c.10107T=	NP_060606.3:p.Phe3369=
NM_018136.5:c.10107T= MANE Select	NP_060606.3:p.Phe3369=
NM_001206846.2:c.5352T=	NP_001193775.1:p.Phe1784=