Canonical Allele Identifier: CA2586964487

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197124231dup , CM000663.2:g.197124231dup	GRCh38
NC_000001.10:g.197093361dup , CM000663.1:g.197093361dup	GRCh37
NC_000001.9:g.195359984dup	NCBI36
NG_015867.1:g.27464dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1311dup
ENST00000367409.9:c.3269dup MANE Select	ENSP00000356379.4:p.Asp1091Ter
ENST00000680112.1:n.1325dup
ENST00000680265.1:c.3269dup	ENSP00000505384.1:p.Asp1091Ter
ENST00000680710.1:c.3269dup	ENSP00000506676.1:p.Asp1091Ter
ENST00000681879.1:c.3269dup	ENSP00000505363.1:p.Asp1091Ter
ENST00000294732.11:c.3269dup	ENSP00000294732.7:p.Asp1091Ter
ENST00000367408.5:c.1019dup	ENSP00000356378.1:p.Asp341Ter
ENST00000367409.8:c.3269dup	ENSP00000356379.4:p.Asp1091Ter
ENST00000612785.1:c.561+19460dup	ENSP00000479244.1:n.561+19460dup
NM_001206846.1:c.3269dup	NP_001193775.1:p.Asp1091Ter
NM_018136.4:c.3269dup	NP_060606.3:p.Asp1091Ter
NM_018136.5:c.3269dup MANE Select	NP_060606.3:p.Asp1091Ter
NM_001206846.2:c.3269dup	NP_001193775.1:p.Asp1091Ter