Canonical Allele Identifier: CA1217926722
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197093191T= , CM000663.2:g.197093191T= GRCh38
NC_000001.10:g.197062321T= , CM000663.1:g.197062321T= GRCh37
NC_000001.9:g.195328944T= NCBI36
NG_015867.1:g.58504A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2442A=
ENST00000367409.9:c.9155A= MANE Select ENSP00000356379.4:p.Gln3052=
ENST00000680265.1:c.9377A= ENSP00000505384.1:p.Gln3126=
ENST00000680710.1:c.9155A= ENSP00000506676.1:p.Gln3052=
ENST00000294732.11:c.4400A= ENSP00000294732.7:p.Gln1467=
ENST00000367408.5:c.2150A= ENSP00000356378.1:p.Gln717=
ENST00000367409.8:c.9155A= ENSP00000356379.4:p.Gln3052=
ENST00000612785.1:c.3113A= ENSP00000479244.1:p.Gln1038=
NM_001206846.1:c.4400A= NP_001193775.1:p.Gln1467=
NM_018136.4:c.9155A= NP_060606.3:p.Gln3052=
NM_018136.5:c.9155A= MANE Select NP_060606.3:p.Gln3052=
NM_001206846.2:c.4400A= NP_001193775.1:p.Gln1467=