Canonical Allele Identifier: CA344021552

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197071608T>C (hg19) ; chr1:g.197102478T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102478T>C , CM000663.2:g.197102478T>C	GRCh38
NC_000001.10:g.197071608T>C , CM000663.1:g.197071608T>C	GRCh37
NC_000001.9:g.195338231T>C	NCBI36
NG_015867.1:g.49217A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6314A>G
ENST00000367409.9:c.6773A>G MANE Select	ENSP00000356379.4:p.His2258Arg
ENST00000680265.1:c.6773A>G	ENSP00000505384.1:p.His2258Arg
ENST00000680710.1:c.6773A>G	ENSP00000506676.1:p.His2258Arg
ENST00000294732.11:c.4066-6314A>G	ENSP00000294732.7:n.4066-6314A>G
ENST00000367408.5:c.1816-6314A>G	ENSP00000356378.1:n.1816-6314A>G
ENST00000367409.8:c.6773A>G	ENSP00000356379.4:p.His2258Arg
ENST00000612785.1:c.731A>G	ENSP00000479244.1:p.His244Arg
NM_001206846.1:c.4066-6314A>G	NP_001193775.1:n.4066-6314A>G
NM_018136.4:c.6773A>G	NP_060606.3:p.His2258Arg
NM_018136.5:c.6773A>G MANE Select	NP_060606.3:p.His2258Arg
NM_001206846.2:c.4066-6314A>G	NP_001193775.1:n.4066-6314A>G