Canonical Allele Identifier: CA1308942
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs754856249

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197091038A>C , CM000663.2:g.197091038A>C GRCh38
NC_000001.10:g.197060168A>C , CM000663.1:g.197060168A>C GRCh37
NC_000001.9:g.195326791A>C NCBI36
NG_015867.1:g.60657T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2735T>G
ENST00000367409.9:c.9448T>G MANE Select ENSP00000356379.4:p.Trp3150Gly
ENST00000680265.1:c.9670T>G ENSP00000505384.1:p.Trp3224Gly
ENST00000680710.1:c.9424T>G ENSP00000506676.1:p.Trp3142Gly
ENST00000294732.11:c.4693T>G ENSP00000294732.7:p.Trp1565Gly
ENST00000367408.5:c.2443T>G ENSP00000356378.1:p.Trp815Gly
ENST00000367409.8:c.9448T>G ENSP00000356379.4:p.Trp3150Gly
ENST00000612785.1:c.3406T>G ENSP00000479244.1:p.Trp1136Gly
NM_001206846.1:c.4693T>G NP_001193775.1:p.Trp1565Gly
NM_018136.4:c.9448T>G NP_060606.3:p.Trp3150Gly
NM_018136.5:c.9448T>G MANE Select NP_060606.3:p.Trp3150Gly
NM_001206846.2:c.4693T>G NP_001193775.1:p.Trp1565Gly