Canonical Allele Identifier: CA645526309

Gene: ASPM

Linked Data

• COSMIC: COSM4663798

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142443dup , CM000663.2:g.197142443dup	GRCh38
NC_000001.10:g.197111573dup , CM000663.1:g.197111573dup	GRCh37
NC_000001.9:g.195378196dup	NCBI36
NG_015867.1:g.9256dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1813dup MANE Select	ENSP00000356379.4:p.Ser605PhefsTer6
ENST00000679766.1:n.2030dup
ENST00000680265.1:c.1813dup	ENSP00000505384.1:p.Ser605PhefsTer6
ENST00000680710.1:c.1813dup	ENSP00000506676.1:p.Ser605PhefsTer6
ENST00000681879.1:c.1813dup	ENSP00000505363.1:p.Ser605PhefsTer6
ENST00000294732.11:c.1813dup	ENSP00000294732.7:p.Ser605PhefsTer6
ENST00000367409.8:c.1813dup	ENSP00000356379.4:p.Ser605PhefsTer6
ENST00000612785.1:c.561+1252dup	ENSP00000479244.1:n.561+1252dup
NM_001206846.1:c.1813dup	NP_001193775.1:p.Ser605PhefsTer6
NM_018136.4:c.1813dup	NP_060606.3:p.Ser605PhefsTer6
NM_018136.5:c.1813dup MANE Select	NP_060606.3:p.Ser605PhefsTer6
NM_001206846.2:c.1813dup	NP_001193775.1:p.Ser605PhefsTer6