Canonical Allele Identifier: CA344007553

Gene: ASPM

Linked Data

• gnomAD v4: 1-197093210-T-C
• MyVariant Identifiers: chr1:g.197062340T>C (hg19) ; chr1:g.197093210T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093210T>C , CM000663.2:g.197093210T>C	GRCh38
NC_000001.10:g.197062340T>C , CM000663.1:g.197062340T>C	GRCh37
NC_000001.9:g.195328963T>C	NCBI36
NG_015867.1:g.58485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2423A>G
ENST00000367409.9:c.9136A>G MANE Select	ENSP00000356379.4:p.Arg3046Gly
ENST00000680265.1:c.9358A>G	ENSP00000505384.1:p.Arg3120Gly
ENST00000680710.1:c.9136A>G	ENSP00000506676.1:p.Arg3046Gly
ENST00000294732.11:c.4381A>G	ENSP00000294732.7:p.Arg1461Gly
ENST00000367408.5:c.2131A>G	ENSP00000356378.1:p.Arg711Gly
ENST00000367409.8:c.9136A>G	ENSP00000356379.4:p.Arg3046Gly
ENST00000612785.1:c.3094A>G	ENSP00000479244.1:p.Arg1032Gly
NM_001206846.1:c.4381A>G	NP_001193775.1:p.Arg1461Gly
NM_018136.4:c.9136A>G	NP_060606.3:p.Arg3046Gly
NM_018136.5:c.9136A>G MANE Select	NP_060606.3:p.Arg3046Gly
NM_001206846.2:c.4381A>G	NP_001193775.1:p.Arg1461Gly