Canonical Allele Identifier: CA1143355895
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197143958_197143962delinsTTTTT , CM000663.2:g.197143958_197143962delinsTTTTT GRCh38
NC_000001.10:g.197113088_197113092delinsTTTTT , CM000663.1:g.197113088_197113092delinsTTTTT GRCh37
NC_000001.9:g.195379711_195379715delinsTTTTT NCBI36
NG_015867.1:g.7733_7737delinsAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.436_440delinsAAAAA MANE Select ENSP00000356379.4:p.Lys146=
ENST00000679766.1:n.653_657delinsAAAAA
ENST00000680265.1:c.436_440delinsAAAAA ENSP00000505384.1:p.Lys146=
ENST00000680710.1:c.436_440delinsAAAAA ENSP00000506676.1:p.Lys146=
ENST00000681879.1:c.436_440delinsAAAAA ENSP00000505363.1:p.Lys146=
ENST00000294732.11:c.436_440delinsAAAAA ENSP00000294732.7:p.Lys146=
ENST00000367409.8:c.436_440delinsAAAAA ENSP00000356379.4:p.Lys146=
ENST00000612785.1:c.436_440delinsAAAAA ENSP00000479244.1:p.Lys146=
NM_001206846.1:c.436_440delinsAAAAA NP_001193775.1:p.Lys146=
NM_018136.4:c.436_440delinsAAAAA NP_060606.3:p.Lys146=
NM_018136.5:c.436_440delinsAAAAA MANE Select NP_060606.3:p.Lys146=
NM_001206846.2:c.436_440delinsAAAAA NP_001193775.1:p.Lys146=