Canonical Allele Identifier: CA344045999
Community Standard Title: NM_018136.5(ASPM):c.2947G>T (p.Glu983Ter)
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197125181C>A , CM000663.2:g.197125181C>A GRCh38
NC_000001.10:g.197094311C>A , CM000663.1:g.197094311C>A GRCh37
NC_000001.9:g.195360934C>A NCBI36
NG_015867.1:g.26514G>T

Transcript Alleles

HGVS Amino-acid Change
NM_018136.5:c.2947G>T MANE Select NP_060606.3:p.Glu983Ter
ENST00000367409.9:c.2947G>T MANE Select ENSP00000356379.4:p.Glu983Ter
NM_001206846.1:c.2947G>T NP_001193775.1:p.Glu983Ter
NM_001206846.2:c.2947G>T NP_001193775.1:p.Glu983Ter
NM_018136.4:c.2947G>T NP_060606.3:p.Glu983Ter
ENST00000294732.11:c.2947G>T ENSP00000294732.7:p.Glu983Ter
ENST00000367408.5:c.697G>T ENSP00000356378.1:p.Glu233Ter
ENST00000367408.6:n.899G>T
ENST00000367409.8:c.2947G>T ENSP00000356379.4:p.Glu983Ter
ENST00000612785.1:c.561+18510G>T ENSP00000479244.1:n.561+18510G>T
ENST00000680112.1:n.1003G>T
ENST00000680265.1:c.2947G>T ENSP00000505384.1:p.Glu983Ter
ENST00000680710.1:c.2947G>T ENSP00000506676.1:p.Glu983Ter
ENST00000681879.1:c.2947G>T ENSP00000505363.1:p.Glu983Ter