Canonical Allele Identifier: CA271086

Gene: ASPM

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102534C>G , CM000663.2:g.197102534C>G	GRCh38
NC_000001.10:g.197071664C>G , CM000663.1:g.197071664C>G	GRCh37
NC_000001.9:g.195338287C>G	NCBI36
NG_015867.1:g.49161G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6370G>C
ENST00000367409.9:c.6717G>C MANE Select	ENSP00000356379.4:p.Leu2239=
ENST00000680265.1:c.6717G>C	ENSP00000505384.1:p.Leu2239=
ENST00000680710.1:c.6717G>C	ENSP00000506676.1:p.Leu2239=
ENST00000294732.11:c.4066-6370G>C	ENSP00000294732.7:n.4066-6370G>C
ENST00000367408.5:c.1816-6370G>C	ENSP00000356378.1:n.1816-6370G>C
ENST00000367409.8:c.6717G>C	ENSP00000356379.4:p.Leu2239=
ENST00000612785.1:c.675G>C	ENSP00000479244.1:p.Leu225=
NM_001206846.1:c.4066-6370G>C	NP_001193775.1:n.4066-6370G>C
NM_018136.4:c.6717G>C	NP_060606.3:p.Leu2239=
NM_018136.5:c.6717G>C MANE Select	NP_060606.3:p.Leu2239=
NM_001206846.2:c.4066-6370G>C	NP_001193775.1:n.4066-6370G>C