Canonical Allele Identifier: CA344001897

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059463G>C (hg19) ; chr1:g.197090333G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090333G>C , CM000663.2:g.197090333G>C	GRCh38
NC_000001.10:g.197059463G>C , CM000663.1:g.197059463G>C	GRCh37
NC_000001.9:g.195326086G>C	NCBI36
NG_015867.1:g.61362C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2979C>G
ENST00000367409.9:c.9692C>G MANE Select	ENSP00000356379.4:p.Ala3231Gly
ENST00000680265.1:c.9914C>G	ENSP00000505384.1:p.Ala3305Gly
ENST00000680710.1:c.9668C>G	ENSP00000506676.1:p.Ala3223Gly
ENST00000294732.11:c.4937C>G	ENSP00000294732.7:p.Ala1646Gly
ENST00000367408.5:c.2687C>G	ENSP00000356378.1:p.Ala896Gly
ENST00000367409.8:c.9692C>G	ENSP00000356379.4:p.Ala3231Gly
ENST00000612785.1:c.3650C>G	ENSP00000479244.1:p.Ala1217Gly
NM_001206846.1:c.4937C>G	NP_001193775.1:p.Ala1646Gly
NM_018136.4:c.9692C>G	NP_060606.3:p.Ala3231Gly
NM_018136.5:c.9692C>G MANE Select	NP_060606.3:p.Ala3231Gly
NM_001206846.2:c.4937C>G	NP_001193775.1:p.Ala1646Gly