Canonical Allele Identifier: CA1309032

Gene: ASPM

Linked Data

• dbSNP Id: rs749481303
• ExAC: 1:197062338 C / T
• gnomAD v2: 1-197062338-C-T
• gnomAD v4: 1-197093208-C-T
• MyVariant Identifiers: chr1:g.197062338C>T (hg19) ; chr1:g.197093208C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093208C>T , CM000663.2:g.197093208C>T	GRCh38
NC_000001.10:g.197062338C>T , CM000663.1:g.197062338C>T	GRCh37
NC_000001.9:g.195328961C>T	NCBI36
NG_015867.1:g.58487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2425G>A
ENST00000367409.9:c.9138G>A MANE Select	ENSP00000356379.4:p.Arg3046=
ENST00000680265.1:c.9360G>A	ENSP00000505384.1:p.Arg3120=
ENST00000680710.1:c.9138G>A	ENSP00000506676.1:p.Arg3046=
ENST00000294732.11:c.4383G>A	ENSP00000294732.7:p.Arg1461=
ENST00000367408.5:c.2133G>A	ENSP00000356378.1:p.Arg711=
ENST00000367409.8:c.9138G>A	ENSP00000356379.4:p.Arg3046=
ENST00000612785.1:c.3096G>A	ENSP00000479244.1:p.Arg1032=
NM_001206846.1:c.4383G>A	NP_001193775.1:p.Arg1461=
NM_018136.4:c.9138G>A	NP_060606.3:p.Arg3046=
NM_018136.5:c.9138G>A MANE Select	NP_060606.3:p.Arg3046=
NM_001206846.2:c.4383G>A	NP_001193775.1:p.Arg1461=