Canonical Allele Identifier: CA1143355795

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093187_197093189delinsTTT , CM000663.2:g.197093187_197093189delinsTTT	GRCh38
NC_000001.10:g.197062317_197062319delinsTTT , CM000663.1:g.197062317_197062319delinsTTT	GRCh37
NC_000001.9:g.195328940_195328942delinsTTT	NCBI36
NG_015867.1:g.58506_58508delinsAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2444_2446delinsAAA
ENST00000367409.9:c.9157_9159delinsAAA MANE Select	ENSP00000356379.4:p.Lys3053=
ENST00000680265.1:c.9379_9381delinsAAA	ENSP00000505384.1:p.Lys3127=
ENST00000680710.1:c.9157_9159delinsAAA	ENSP00000506676.1:p.Lys3053=
ENST00000294732.11:c.4402_4404delinsAAA	ENSP00000294732.7:p.Lys1468=
ENST00000367408.5:c.2152_2154delinsAAA	ENSP00000356378.1:p.Lys718=
ENST00000367409.8:c.9157_9159delinsAAA	ENSP00000356379.4:p.Lys3053=
ENST00000612785.1:c.3115_3117delinsAAA	ENSP00000479244.1:p.Lys1039=
NM_001206846.1:c.4402_4404delinsAAA	NP_001193775.1:p.Lys1468=
NM_018136.4:c.9157_9159delinsAAA	NP_060606.3:p.Lys3053=
NM_018136.5:c.9157_9159delinsAAA MANE Select	NP_060606.3:p.Lys3053=
NM_001206846.2:c.4402_4404delinsAAA	NP_001193775.1:p.Lys1468=