Canonical Allele Identifier: CA1149105486

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143654T= , CM000663.2:g.197143654T=	GRCh38
NC_000001.10:g.197112784T= , CM000663.1:g.197112784T=	GRCh37
NC_000001.9:g.195379407T=	NCBI36
NG_015867.1:g.8041A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.598A= MANE Select	ENSP00000356379.4:p.Met200=
ENST00000679766.1:n.815A=
ENST00000680265.1:c.598A=	ENSP00000505384.1:p.Met200=
ENST00000680710.1:c.598A=	ENSP00000506676.1:p.Met200=
ENST00000681879.1:c.598A=	ENSP00000505363.1:p.Met200=
ENST00000294732.11:c.598A=	ENSP00000294732.7:p.Met200=
ENST00000367409.8:c.598A=	ENSP00000356379.4:p.Met200=
ENST00000612785.1:c.561+37A=	ENSP00000479244.1:n.561+37A=
NM_001206846.1:c.598A=	NP_001193775.1:p.Met200=
NM_018136.4:c.598A=	NP_060606.3:p.Met200=
NM_018136.5:c.598A= MANE Select	NP_060606.3:p.Met200=
NM_001206846.2:c.598A=	NP_001193775.1:p.Met200=