Canonical Allele Identifier: CA1217929667

Gene: ASPM

Linked Data

• dbSNP Id: rs1657135336

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197100728dup , CM000663.2:g.197100728dup	GRCh38
NC_000001.10:g.197069858dup , CM000663.1:g.197069858dup	GRCh37
NC_000001.9:g.195336481dup	NCBI36
NG_015867.1:g.50967dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-4564dup
ENST00000367409.9:c.8523dup MANE Select	ENSP00000356379.4:p.Arg2842ThrfsTer30
ENST00000680265.1:c.8523dup	ENSP00000505384.1:p.Arg2842ThrfsTer30
ENST00000680710.1:c.8523dup	ENSP00000506676.1:p.Arg2842ThrfsTer30
ENST00000294732.11:c.4066-4564dup	ENSP00000294732.7:n.4066-4564dup
ENST00000367408.5:c.1816-4564dup	ENSP00000356378.1:n.1816-4564dup
ENST00000367409.8:c.8523dup	ENSP00000356379.4:p.Arg2842ThrfsTer30
ENST00000612785.1:c.2481dup	ENSP00000479244.1:p.Arg828ThrfsTer30
NM_001206846.1:c.4066-4564dup	NP_001193775.1:n.4066-4564dup
NM_018136.4:c.8523dup	NP_060606.3:p.Arg2842ThrfsTer30
NM_018136.5:c.8523dup MANE Select	NP_060606.3:p.Arg2842ThrfsTer30
NM_001206846.2:c.4066-4564dup	NP_001193775.1:n.4066-4564dup