Canonical Allele Identifier: CA1143355787

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090335_197090342delinsTTTAATTT , CM000663.2:g.197090335_197090342delinsTTTAATTT	GRCh38
NC_000001.10:g.197059465_197059472delinsTTTAATTT , CM000663.1:g.197059465_197059472delinsTTTAATTT	GRCh37
NC_000001.9:g.195326088_195326095delinsTTTAATTT	NCBI36
NG_015867.1:g.61353_61360delinsAAATTAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2970_2977delinsAAATTAAA
ENST00000367409.9:c.9683_9690delinsAAATTAAA MANE Select	ENSP00000356379.4:p.Lys3228=
ENST00000680265.1:c.9905_9912delinsAAATTAAA	ENSP00000505384.1:p.Lys3302=
ENST00000680710.1:c.9659_9666delinsAAATTAAA	ENSP00000506676.1:p.Lys3220=
ENST00000294732.11:c.4928_4935delinsAAATTAAA	ENSP00000294732.7:p.Lys1643=
ENST00000367408.5:c.2678_2685delinsAAATTAAA	ENSP00000356378.1:p.Lys893=
ENST00000367409.8:c.9683_9690delinsAAATTAAA	ENSP00000356379.4:p.Lys3228=
ENST00000612785.1:c.3641_3648delinsAAATTAAA	ENSP00000479244.1:p.Lys1214=
NM_001206846.1:c.4928_4935delinsAAATTAAA	NP_001193775.1:p.Lys1643=
NM_018136.4:c.9683_9690delinsAAATTAAA	NP_060606.3:p.Lys3228=
NM_018136.5:c.9683_9690delinsAAATTAAA MANE Select	NP_060606.3:p.Lys3228=
NM_001206846.2:c.4928_4935delinsAAATTAAA	NP_001193775.1:p.Lys1643=