Canonical Allele Identifier: CA645523001

Gene: ASPM

Linked Data

• COSMIC: COSM5832443

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103638_197103639insTAT , CM000663.2:g.197103638_197103639insTAT	GRCh38
NC_000001.10:g.197072768_197072769insTAT , CM000663.1:g.197072768_197072769insTAT	GRCh37
NC_000001.9:g.195339391_195339392insTAT	NCBI36
NG_015867.1:g.48056_48057insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7475_2108-7474insATA
ENST00000367409.9:c.5612_5613insATA MANE Select	ENSP00000356379.4:p.Phe1871delinsLeuTyr
ENST00000680265.1:c.5612_5613insATA	ENSP00000505384.1:p.Phe1871delinsLeuTyr
ENST00000680710.1:c.5612_5613insATA	ENSP00000506676.1:p.Phe1871delinsLeuTyr
ENST00000294732.11:c.4066-7475_4066-7474insATA	ENSP00000294732.7:n.4066-7475_4066-7474insATA
ENST00000367408.5:c.1816-7475_1816-7474insATA	ENSP00000356378.1:n.1816-7475_1816-7474insATA
ENST00000367409.8:c.5612_5613insATA	ENSP00000356379.4:p.Phe1871delinsLeuTyr
ENST00000612785.1:c.562-992_562-991insATA	ENSP00000479244.1:n.562-992_562-991insATA
NM_001206846.1:c.4066-7475_4066-7474insATA	NP_001193775.1:n.4066-7475_4066-7474insATA
NM_018136.4:c.5612_5613insATA	NP_060606.3:p.Phe1871delinsLeuTyr
NM_018136.5:c.5612_5613insATA MANE Select	NP_060606.3:p.Phe1871delinsLeuTyr
NM_001206846.2:c.4066-7475_4066-7474insATA	NP_001193775.1:n.4066-7475_4066-7474insATA