Canonical Allele Identifier: CA344007057

Gene: ASPM

Linked Data

• dbSNP Id: rs1558324122
• MyVariant Identifiers: chr1:g.197062270C>G (hg19) ; chr1:g.197093140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093140C>G , CM000663.2:g.197093140C>G	GRCh38
NC_000001.10:g.197062270C>G , CM000663.1:g.197062270C>G	GRCh37
NC_000001.9:g.195328893C>G	NCBI36
NG_015867.1:g.58555G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2493G>C
ENST00000367409.9:c.9206G>C MANE Select	ENSP00000356379.4:p.Gly3069Ala
ENST00000680265.1:c.9428G>C	ENSP00000505384.1:p.Gly3143Ala
ENST00000680710.1:c.9206G>C	ENSP00000506676.1:p.Gly3069Ala
ENST00000294732.11:c.4451G>C	ENSP00000294732.7:p.Gly1484Ala
ENST00000367408.5:c.2201G>C	ENSP00000356378.1:p.Gly734Ala
ENST00000367409.8:c.9206G>C	ENSP00000356379.4:p.Gly3069Ala
ENST00000612785.1:c.3164G>C	ENSP00000479244.1:p.Gly1055Ala
NM_001206846.1:c.4451G>C	NP_001193775.1:p.Gly1484Ala
NM_018136.4:c.9206G>C	NP_060606.3:p.Gly3069Ala
NM_018136.5:c.9206G>C MANE Select	NP_060606.3:p.Gly3069Ala
NM_001206846.2:c.4451G>C	NP_001193775.1:p.Gly1484Ala