Canonical Allele Identifier: CA1217939303
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197124214_197124218delinsTATTA , CM000663.2:g.197124214_197124218delinsTATTA GRCh38
NC_000001.10:g.197093344_197093348delinsTATTA , CM000663.1:g.197093344_197093348delinsTATTA GRCh37
NC_000001.9:g.195359967_195359971delinsTATTA NCBI36
NG_015867.1:g.27477_27481delinsTAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1324_1328delinsTAATA
ENST00000367409.9:c.3282_3286delinsTAATA MANE Select ENSP00000356379.4:p.Ile1094=
ENST00000680112.1:n.1338_1342delinsTAATA
ENST00000680265.1:c.3282_3286delinsTAATA ENSP00000505384.1:p.Ile1094=
ENST00000680710.1:c.3282_3286delinsTAATA ENSP00000506676.1:p.Ile1094=
ENST00000681879.1:c.3282_3286delinsTAATA ENSP00000505363.1:p.Ile1094=
ENST00000294732.11:c.3282_3286delinsTAATA ENSP00000294732.7:p.Ile1094=
ENST00000367408.5:c.1032_1036delinsTAATA ENSP00000356378.1:p.Ile344=
ENST00000367409.8:c.3282_3286delinsTAATA ENSP00000356379.4:p.Ile1094=
ENST00000612785.1:c.561+19473_561+19477delinsTAATA ENSP00000479244.1:n.561+19473_561+19477delinsTAATA
NM_001206846.1:c.3282_3286delinsTAATA NP_001193775.1:p.Ile1094=
NM_018136.4:c.3282_3286delinsTAATA NP_060606.3:p.Ile1094=
NM_018136.5:c.3282_3286delinsTAATA MANE Select NP_060606.3:p.Ile1094=
NM_001206846.2:c.3282_3286delinsTAATA NP_001193775.1:p.Ile1094=