Canonical Allele Identifier: CA1143355782

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090236A= , CM000663.2:g.197090236A=	GRCh38
NC_000001.10:g.197059366A= , CM000663.1:g.197059366A=	GRCh37
NC_000001.9:g.195325989A=	NCBI36
NG_015867.1:g.61459T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3076T=
ENST00000367409.9:c.9789T= MANE Select	ENSP00000356379.4:p.Tyr3263=
ENST00000680265.1:c.10011T=	ENSP00000505384.1:p.Tyr3337=
ENST00000680710.1:c.9765T=	ENSP00000506676.1:p.Tyr3255=
ENST00000294732.11:c.5034T=	ENSP00000294732.7:p.Tyr1678=
ENST00000367408.5:c.2784T=	ENSP00000356378.1:p.Tyr928=
ENST00000367409.8:c.9789T=	ENSP00000356379.4:p.Tyr3263=
ENST00000612785.1:c.3747T=	ENSP00000479244.1:p.Tyr1249=
NM_001206846.1:c.5034T=	NP_001193775.1:p.Tyr1678=
NM_018136.4:c.9789T=	NP_060606.3:p.Tyr3263=
NM_018136.5:c.9789T= MANE Select	NP_060606.3:p.Tyr3263=
NM_001206846.2:c.5034T=	NP_001193775.1:p.Tyr1678=