Canonical Allele Identifier: CA343996950

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057347A>C (hg19) ; chr1:g.197088217A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088217A>C , CM000663.2:g.197088217A>C	GRCh38
NC_000001.10:g.197057347A>C , CM000663.1:g.197057347A>C	GRCh37
NC_000001.9:g.195323970A>C	NCBI36
NG_015867.1:g.63478T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3448+39T>G
ENST00000367409.9:c.10161+39T>G MANE Select	ENSP00000356379.4:n.10161+39T>G
ENST00000680265.1:c.10383+39T>G	ENSP00000505384.1:n.10383+39T>G
ENST00000680710.1:c.10137+39T>G	ENSP00000506676.1:n.10137+39T>G
ENST00000294732.11:c.5406+39T>G	ENSP00000294732.7:n.5406+39T>G
ENST00000367408.5:c.3156+39T>G	ENSP00000356378.1:n.3156+39T>G
ENST00000367409.8:c.10161+39T>G	ENSP00000356379.4:n.10161+39T>G
ENST00000612785.1:c.4158T>G	ENSP00000479244.1:p.Phe1386Leu
NM_001206846.1:c.5406+39T>G	NP_001193775.1:n.5406+39T>G
NM_018136.4:c.10161+39T>G	NP_060606.3:n.10161+39T>G
NM_018136.5:c.10161+39T>G MANE Select	NP_060606.3:n.10161+39T>G
NM_001206846.2:c.5406+39T>G	NP_001193775.1:n.5406+39T>G