Canonical Allele Identifier: CA343997996

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057462G>C (hg19) ; chr1:g.197088332G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088332G>C , CM000663.2:g.197088332G>C	GRCh38
NC_000001.10:g.197057462G>C , CM000663.1:g.197057462G>C	GRCh37
NC_000001.9:g.195324085G>C	NCBI36
NG_015867.1:g.63363C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3372C>G
ENST00000367409.9:c.10085C>G MANE Select	ENSP00000356379.4:p.Ala3362Gly
ENST00000680265.1:c.10307C>G	ENSP00000505384.1:p.Ala3436Gly
ENST00000680710.1:c.10061C>G	ENSP00000506676.1:p.Ala3354Gly
ENST00000294732.11:c.5330C>G	ENSP00000294732.7:p.Ala1777Gly
ENST00000367408.5:c.3080C>G	ENSP00000356378.1:p.Ala1027Gly
ENST00000367409.8:c.10085C>G	ENSP00000356379.4:p.Ala3362Gly
ENST00000612785.1:c.4043C>G	ENSP00000479244.1:p.Ala1348Gly
NM_001206846.1:c.5330C>G	NP_001193775.1:p.Ala1777Gly
NM_018136.4:c.10085C>G	NP_060606.3:p.Ala3362Gly
NM_018136.5:c.10085C>G MANE Select	NP_060606.3:p.Ala3362Gly
NM_001206846.2:c.5330C>G	NP_001193775.1:p.Ala1777Gly