Canonical Allele Identifier: CA1217945679

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142720_197142722delinsTCA , CM000663.2:g.197142720_197142722delinsTCA	GRCh38
NC_000001.10:g.197111850_197111852delinsTCA , CM000663.1:g.197111850_197111852delinsTCA	GRCh37
NC_000001.9:g.195378473_195378475delinsTCA	NCBI36
NG_015867.1:g.8973_8975delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1530_1532delinsTGA MANE Select	ENSP00000356379.4:p.Thr510=
ENST00000679766.1:n.1747_1749delinsTGA
ENST00000680265.1:c.1530_1532delinsTGA	ENSP00000505384.1:p.Thr510=
ENST00000680710.1:c.1530_1532delinsTGA	ENSP00000506676.1:p.Thr510=
ENST00000681879.1:c.1530_1532delinsTGA	ENSP00000505363.1:p.Thr510=
ENST00000294732.11:c.1530_1532delinsTGA	ENSP00000294732.7:p.Thr510=
ENST00000367409.8:c.1530_1532delinsTGA	ENSP00000356379.4:p.Thr510=
ENST00000612785.1:c.561+969_561+971delinsTGA	ENSP00000479244.1:n.561+969_561+971delinsTGA
NM_001206846.1:c.1530_1532delinsTGA	NP_001193775.1:p.Thr510=
NM_018136.4:c.1530_1532delinsTGA	NP_060606.3:p.Thr510=
NM_018136.5:c.1530_1532delinsTGA MANE Select	NP_060606.3:p.Thr510=
NM_001206846.2:c.1530_1532delinsTGA	NP_001193775.1:p.Thr510=