Canonical Allele Identifier: CA1217946616

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143447_197143449delinsCTT , CM000663.2:g.197143447_197143449delinsCTT	GRCh38
NC_000001.10:g.197112577_197112579delinsCTT , CM000663.1:g.197112577_197112579delinsCTT	GRCh37
NC_000001.9:g.195379200_195379202delinsCTT	NCBI36
NG_015867.1:g.8246_8248delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.803_805delinsAAG MANE Select	ENSP00000356379.4:p.Lys268=
ENST00000679766.1:n.1020_1022delinsAAG
ENST00000680265.1:c.803_805delinsAAG	ENSP00000505384.1:p.Lys268=
ENST00000680710.1:c.803_805delinsAAG	ENSP00000506676.1:p.Lys268=
ENST00000681879.1:c.803_805delinsAAG	ENSP00000505363.1:p.Lys268=
ENST00000294732.11:c.803_805delinsAAG	ENSP00000294732.7:p.Lys268=
ENST00000367409.8:c.803_805delinsAAG	ENSP00000356379.4:p.Lys268=
ENST00000612785.1:c.561+242_561+244delinsAAG	ENSP00000479244.1:n.561+242_561+244delinsAAG
NM_001206846.1:c.803_805delinsAAG	NP_001193775.1:p.Lys268=
NM_018136.4:c.803_805delinsAAG	NP_060606.3:p.Lys268=
NM_018136.5:c.803_805delinsAAG MANE Select	NP_060606.3:p.Lys268=
NM_001206846.2:c.803_805delinsAAG	NP_001193775.1:p.Lys268=