Canonical Allele Identifier: CA1217946046
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142985_197142992delinsGGACTTGA , CM000663.2:g.197142985_197142992delinsGGACTTGA GRCh38
NC_000001.10:g.197112115_197112122delinsGGACTTGA , CM000663.1:g.197112115_197112122delinsGGACTTGA GRCh37
NC_000001.9:g.195378738_195378745delinsGGACTTGA NCBI36
NG_015867.1:g.8703_8710delinsTCAAGTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1260_1267delinsTCAAGTCC MANE Select ENSP00000356379.4:p.Ser420=
ENST00000679766.1:n.1477_1484delinsTCAAGTCC
ENST00000680265.1:c.1260_1267delinsTCAAGTCC ENSP00000505384.1:p.Ser420=
ENST00000680710.1:c.1260_1267delinsTCAAGTCC ENSP00000506676.1:p.Ser420=
ENST00000681879.1:c.1260_1267delinsTCAAGTCC ENSP00000505363.1:p.Ser420=
ENST00000294732.11:c.1260_1267delinsTCAAGTCC ENSP00000294732.7:p.Ser420=
ENST00000367409.8:c.1260_1267delinsTCAAGTCC ENSP00000356379.4:p.Ser420=
ENST00000612785.1:c.561+699_561+706delinsTCAAGTCC ENSP00000479244.1:n.561+699_561+706delins...
NM_001206846.1:c.1260_1267delinsTCAAGTCC NP_001193775.1:p.Ser420=
NM_018136.4:c.1260_1267delinsTCAAGTCC NP_060606.3:p.Ser420=
NM_018136.5:c.1260_1267delinsTCAAGTCC MANE Select NP_060606.3:p.Ser420=
NM_001206846.2:c.1260_1267delinsTCAAGTCC NP_001193775.1:p.Ser420=