Canonical Allele Identifier: CA1217923496

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088293_197088296delinsAAAC , CM000663.2:g.197088293_197088296delinsAAAC	GRCh38
NC_000001.10:g.197057423_197057426delinsAAAC , CM000663.1:g.197057423_197057426delinsAAAC	GRCh37
NC_000001.9:g.195324046_195324049delinsAAAC	NCBI36
NG_015867.1:g.63399_63402delinsGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3408_3411delinsGTTT
ENST00000367409.9:c.10121_10124delinsGTTT MANE Select	ENSP00000356379.4:p.Cys3374=
ENST00000680265.1:c.10343_10346delinsGTTT	ENSP00000505384.1:p.Cys3448=
ENST00000680710.1:c.10097_10100delinsGTTT	ENSP00000506676.1:p.Cys3366=
ENST00000294732.11:c.5366_5369delinsGTTT	ENSP00000294732.7:p.Cys1789=
ENST00000367408.5:c.3116_3119delinsGTTT	ENSP00000356378.1:p.Cys1039=
ENST00000367409.8:c.10121_10124delinsGTTT	ENSP00000356379.4:p.Cys3374=
ENST00000612785.1:c.4079_4082delinsGTTT	ENSP00000479244.1:p.Cys1360=
NM_001206846.1:c.5366_5369delinsGTTT	NP_001193775.1:p.Cys1789=
NM_018136.4:c.10121_10124delinsGTTT	NP_060606.3:p.Cys3374=
NM_018136.5:c.10121_10124delinsGTTT MANE Select	NP_060606.3:p.Cys3374=
NM_001206846.2:c.5366_5369delinsGTTT	NP_001193775.1:p.Cys1789=