Canonical Allele Identifier: CA422673069

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197062281G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093151G>T , CM000663.2:g.197093151G>T	GRCh38
NC_000001.10:g.197062281G>T , CM000663.1:g.197062281G>T	GRCh37
NC_000001.9:g.195328904G>T	NCBI36
NG_015867.1:g.58544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2482C>A
ENST00000367409.9:c.9195C>A MANE Select	ENSP00000356379.4:p.Ala3065=
ENST00000680265.1:c.9417C>A	ENSP00000505384.1:p.Ala3139=
ENST00000680710.1:c.9195C>A	ENSP00000506676.1:p.Ala3065=
ENST00000294732.11:c.4440C>A	ENSP00000294732.7:p.Ala1480=
ENST00000367408.5:c.2190C>A	ENSP00000356378.1:p.Ala730=
ENST00000367409.8:c.9195C>A	ENSP00000356379.4:p.Ala3065=
ENST00000612785.1:c.3153C>A	ENSP00000479244.1:p.Ala1051=
NM_001206846.1:c.4440C>A	NP_001193775.1:p.Ala1480=
NM_018136.4:c.9195C>A	NP_060606.3:p.Ala3065=
NM_018136.5:c.9195C>A MANE Select	NP_060606.3:p.Ala3065=
NM_001206846.2:c.4440C>A	NP_001193775.1:p.Ala1480=