Canonical Allele Identifier: CA1217925899

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091038_197091040delinsATC , CM000663.2:g.197091038_197091040delinsATC	GRCh38
NC_000001.10:g.197060168_197060170delinsATC , CM000663.1:g.197060168_197060170delinsATC	GRCh37
NC_000001.9:g.195326791_195326793delinsATC	NCBI36
NG_015867.1:g.60655_60657delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2733_2735delinsGAT
ENST00000367409.9:c.9446_9448delinsGAT MANE Select	ENSP00000356379.4:p.Arg3149=
ENST00000680265.1:c.9668_9670delinsGAT	ENSP00000505384.1:p.Arg3223=
ENST00000680710.1:c.9422_9424delinsGAT	ENSP00000506676.1:p.Arg3141=
ENST00000294732.11:c.4691_4693delinsGAT	ENSP00000294732.7:p.Arg1564=
ENST00000367408.5:c.2441_2443delinsGAT	ENSP00000356378.1:p.Arg814=
ENST00000367409.8:c.9446_9448delinsGAT	ENSP00000356379.4:p.Arg3149=
ENST00000612785.1:c.3404_3406delinsGAT	ENSP00000479244.1:p.Arg1135=
NM_001206846.1:c.4691_4693delinsGAT	NP_001193775.1:p.Arg1564=
NM_018136.4:c.9446_9448delinsGAT	NP_060606.3:p.Arg3149=
NM_018136.5:c.9446_9448delinsGAT MANE Select	NP_060606.3:p.Arg3149=
NM_001206846.2:c.4691_4693delinsGAT	NP_001193775.1:p.Arg1564=