Canonical Allele Identifier: CA422672462

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060094A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090964A>C , CM000663.2:g.197090964A>C	GRCh38
NC_000001.10:g.197060094A>C , CM000663.1:g.197060094A>C	GRCh37
NC_000001.9:g.195326717A>C	NCBI36
NG_015867.1:g.60731T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2809T>G
ENST00000367409.9:c.9522T>G MANE Select	ENSP00000356379.4:p.Gly3174=
ENST00000680265.1:c.9744T>G	ENSP00000505384.1:p.Gly3248=
ENST00000680710.1:c.9498T>G	ENSP00000506676.1:p.Gly3166=
ENST00000294732.11:c.4767T>G	ENSP00000294732.7:p.Gly1589=
ENST00000367408.5:c.2517T>G	ENSP00000356378.1:p.Gly839=
ENST00000367409.8:c.9522T>G	ENSP00000356379.4:p.Gly3174=
ENST00000612785.1:c.3480T>G	ENSP00000479244.1:p.Gly1160=
NM_001206846.1:c.4767T>G	NP_001193775.1:p.Gly1589=
NM_018136.4:c.9522T>G	NP_060606.3:p.Gly3174=
NM_018136.5:c.9522T>G MANE Select	NP_060606.3:p.Gly3174=
NM_001206846.2:c.4767T>G	NP_001193775.1:p.Gly1589=