Canonical Allele Identifier: CA344027351
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs1177002907

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197104069T>C , CM000663.2:g.197104069T>C GRCh38
NC_000001.10:g.197073199T>C , CM000663.1:g.197073199T>C GRCh37
NC_000001.9:g.195339822T>C NCBI36
NG_015867.1:g.47626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-7905A>G
ENST00000367409.9:c.5182A>G MANE Select ENSP00000356379.4:p.Met1728Val
ENST00000680265.1:c.5182A>G ENSP00000505384.1:p.Met1728Val
ENST00000680710.1:c.5182A>G ENSP00000506676.1:p.Met1728Val
ENST00000294732.11:c.4066-7905A>G ENSP00000294732.7:n.4066-7905A>G
ENST00000367408.5:c.1816-7905A>G ENSP00000356378.1:n.1816-7905A>G
ENST00000367409.8:c.5182A>G ENSP00000356379.4:p.Met1728Val
ENST00000612785.1:c.562-1422A>G ENSP00000479244.1:n.562-1422A>G
NM_001206846.1:c.4066-7905A>G NP_001193775.1:n.4066-7905A>G
NM_018136.4:c.5182A>G NP_060606.3:p.Met1728Val
NM_018136.5:c.5182A>G MANE Select NP_060606.3:p.Met1728Val
NM_001206846.2:c.4066-7905A>G NP_001193775.1:n.4066-7905A>G