Canonical Allele Identifier: CA1217926727

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093218T= , CM000663.2:g.197093218T=	GRCh38
NC_000001.10:g.197062348T= , CM000663.1:g.197062348T=	GRCh37
NC_000001.9:g.195328971T=	NCBI36
NG_015867.1:g.58477A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2415A=
ENST00000367409.9:c.9128A= MANE Select	ENSP00000356379.4:p.Tyr3043=
ENST00000680265.1:c.9350A=	ENSP00000505384.1:p.Tyr3117=
ENST00000680710.1:c.9128A=	ENSP00000506676.1:p.Tyr3043=
ENST00000294732.11:c.4373A=	ENSP00000294732.7:p.Tyr1458=
ENST00000367408.5:c.2123A=	ENSP00000356378.1:p.Tyr708=
ENST00000367409.8:c.9128A=	ENSP00000356379.4:p.Tyr3043=
ENST00000612785.1:c.3086A=	ENSP00000479244.1:p.Tyr1029=
NM_001206846.1:c.4373A=	NP_001193775.1:p.Tyr1458=
NM_018136.4:c.9128A=	NP_060606.3:p.Tyr3043=
NM_018136.5:c.9128A= MANE Select	NP_060606.3:p.Tyr3043=
NM_001206846.2:c.4373A=	NP_001193775.1:p.Tyr1458=