Canonical Allele Identifier: CA1148224797

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088317C= , CM000663.2:g.197088317C=	GRCh38
NC_000001.10:g.197057447C= , CM000663.1:g.197057447C=	GRCh37
NC_000001.9:g.195324070C=	NCBI36
NG_015867.1:g.63378G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3387G=
ENST00000367409.9:c.10100G= MANE Select	ENSP00000356379.4:p.Ser3367=
ENST00000680265.1:c.10322G=	ENSP00000505384.1:p.Ser3441=
ENST00000680710.1:c.10076G=	ENSP00000506676.1:p.Ser3359=
ENST00000294732.11:c.5345G=	ENSP00000294732.7:p.Ser1782=
ENST00000367408.5:c.3095G=	ENSP00000356378.1:p.Ser1032=
ENST00000367409.8:c.10100G=	ENSP00000356379.4:p.Ser3367=
ENST00000612785.1:c.4058G=	ENSP00000479244.1:p.Ser1353=
NM_001206846.1:c.5345G=	NP_001193775.1:p.Ser1782=
NM_018136.4:c.10100G=	NP_060606.3:p.Ser3367=
NM_018136.5:c.10100G= MANE Select	NP_060606.3:p.Ser3367=
NM_001206846.2:c.5345G=	NP_001193775.1:p.Ser1782=