Canonical Allele Identifier: CA422806522

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197072032_197072033insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102903dup , CM000663.2:g.197102903dup	GRCh38
NC_000001.10:g.197072033dup , CM000663.1:g.197072033dup	GRCh37
NC_000001.9:g.195338656dup	NCBI36
NG_015867.1:g.48792dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6739dup
ENST00000367409.9:c.6348dup MANE Select	ENSP00000356379.4:p.His2117AlafsTer8
ENST00000680265.1:c.6348dup	ENSP00000505384.1:p.His2117AlafsTer8
ENST00000680710.1:c.6348dup	ENSP00000506676.1:p.His2117AlafsTer8
ENST00000294732.11:c.4066-6739dup	ENSP00000294732.7:n.4066-6739dup
ENST00000367408.5:c.1816-6739dup	ENSP00000356378.1:n.1816-6739dup
ENST00000367409.8:c.6348dup	ENSP00000356379.4:p.His2117AlafsTer8
ENST00000612785.1:c.562-256dup	ENSP00000479244.1:n.562-256dup
NM_001206846.1:c.4066-6739dup	NP_001193775.1:n.4066-6739dup
NM_018136.4:c.6348dup	NP_060606.3:p.His2117AlafsTer8
NM_018136.5:c.6348dup MANE Select	NP_060606.3:p.His2117AlafsTer8
NM_001206846.2:c.4066-6739dup	NP_001193775.1:n.4066-6739dup