Canonical Allele Identifier: CA1217945827

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142840_197142843delinsTTAG , CM000663.2:g.197142840_197142843delinsTTAG	GRCh38
NC_000001.10:g.197111970_197111973delinsTTAG , CM000663.1:g.197111970_197111973delinsTTAG	GRCh37
NC_000001.9:g.195378593_195378596delinsTTAG	NCBI36
NG_015867.1:g.8852_8855delinsCTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367409.9:c.1409_1412delinsCTAA MANE Select	ENSP00000356379.4:p.Pro470=
ENST00000679766.1:n.1626_1629delinsCTAA
ENST00000680265.1:c.1409_1412delinsCTAA	ENSP00000505384.1:p.Pro470=
ENST00000680710.1:c.1409_1412delinsCTAA	ENSP00000506676.1:p.Pro470=
ENST00000681879.1:c.1409_1412delinsCTAA	ENSP00000505363.1:p.Pro470=
ENST00000294732.11:c.1409_1412delinsCTAA	ENSP00000294732.7:p.Pro470=
ENST00000367409.8:c.1409_1412delinsCTAA	ENSP00000356379.4:p.Pro470=
ENST00000612785.1:c.561+848_561+851delinsCTAA	ENSP00000479244.1:n.561+848_561+851delins...
NM_001206846.1:c.1409_1412delinsCTAA	NP_001193775.1:p.Pro470=
NM_018136.4:c.1409_1412delinsCTAA	NP_060606.3:p.Pro470=
NM_018136.5:c.1409_1412delinsCTAA MANE Select	NP_060606.3:p.Pro470=
NM_001206846.2:c.1409_1412delinsCTAA	NP_001193775.1:p.Pro470=