Canonical Allele Identifier: CA344014954
Gene: ASPM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142578A>C , CM000663.2:g.197142578A>C GRCh38
NC_000001.10:g.197111708A>C , CM000663.1:g.197111708A>C GRCh37
NC_000001.9:g.195378331A>C NCBI36
NG_015867.1:g.9117T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1674T>G MANE Select ENSP00000356379.4:p.Tyr558Ter
ENST00000679766.1:n.1891T>G
ENST00000680265.1:c.1674T>G ENSP00000505384.1:p.Tyr558Ter
ENST00000680710.1:n.1674T>G ENSP00000506676.1:p.Tyr558Ter
ENST00000681879.1:n.1674T>G ENSP00000505363.1:p.Tyr558Ter
ENST00000294732.11:c.1674T>G ENSP00000294732.7:p.Tyr558Ter
ENST00000367409.8:c.1674T>G ENSP00000356379.4:p.Tyr558Ter
ENST00000612785.1:c.561+1113T>G ENSP00000479244.1:n.561+1113T>G
NM_001206846.1:c.1674T>G NP_001193775.1:p.Tyr558Ter
NM_018136.4:c.1674T>G NP_060606.3:p.Tyr558Ter
NM_018136.5:c.1674T>G MANE Select NP_060606.3:p.Tyr558Ter
NM_001206846.2:c.1674T>G NP_001193775.1:p.Tyr558Ter