Canonical Allele Identifier: CA1217939645
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197125062T= , CM000663.2:g.197125062T= GRCh38
NC_000001.10:g.197094192T= , CM000663.1:g.197094192T= GRCh37
NC_000001.9:g.195360815T= NCBI36
NG_015867.1:g.26633A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.1018A=
ENST00000367409.9:c.3066A= MANE Select ENSP00000356379.4:p.Glu1022=
ENST00000680112.1:n.1122A=
ENST00000680265.1:c.3066A= ENSP00000505384.1:p.Glu1022=
ENST00000680710.1:c.3066A= ENSP00000506676.1:p.Glu1022=
ENST00000681879.1:c.3066A= ENSP00000505363.1:p.Glu1022=
ENST00000294732.11:c.3066A= ENSP00000294732.7:p.Glu1022=
ENST00000367408.5:c.816A= ENSP00000356378.1:p.Glu272=
ENST00000367409.8:c.3066A= ENSP00000356379.4:p.Glu1022=
ENST00000612785.1:c.561+18629A= ENSP00000479244.1:n.561+18629A=
NM_001206846.1:c.3066A= NP_001193775.1:p.Glu1022=
NM_018136.4:c.3066A= NP_060606.3:p.Glu1022=
NM_018136.5:c.3066A= MANE Select NP_060606.3:p.Glu1022=
NM_001206846.2:c.3066A= NP_001193775.1:p.Glu1022=