Canonical Allele Identifier: CA1139844602

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101771A= , CM000663.2:g.197101771A=	GRCh38
NC_000001.10:g.197070901A= , CM000663.1:g.197070901A=	GRCh37
NC_000001.9:g.195337524A=	NCBI36
NG_015867.1:g.49924T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-5607T=
ENST00000367409.9:c.7480T= MANE Select	ENSP00000356379.4:p.Tyr2494=
ENST00000680265.1:c.7480T=	ENSP00000505384.1:p.Tyr2494=
ENST00000680710.1:c.7480T=	ENSP00000506676.1:p.Tyr2494=
ENST00000294732.11:c.4066-5607T=	ENSP00000294732.7:n.4066-5607T=
ENST00000367408.5:c.1816-5607T=	ENSP00000356378.1:n.1816-5607T=
ENST00000367409.8:c.7480T=	ENSP00000356379.4:p.Tyr2494=
ENST00000612785.1:c.1438T=	ENSP00000479244.1:p.Tyr480=
NM_001206846.1:c.4066-5607T=	NP_001193775.1:n.4066-5607T=
NM_018136.4:c.7480T=	NP_060606.3:p.Tyr2494=
NM_018136.5:c.7480T= MANE Select	NP_060606.3:p.Tyr2494=
NM_001206846.2:c.4066-5607T=	NP_001193775.1:n.4066-5607T=