Canonical Allele Identifier: CA1217938490
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197122093_197122097delinsGTACT , CM000663.2:g.197122093_197122097delinsGTACT GRCh38
NC_000001.10:g.197091223_197091227delinsGTACT , CM000663.1:g.197091223_197091227delinsGTACT GRCh37
NC_000001.9:g.195357846_195357850delinsGTACT NCBI36
NG_015867.1:g.29598_29602delinsAGTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1784-54_1784-50delinsAGTAC
ENST00000367409.9:c.3742-54_3742-50delinsAGTAC MANE Select ENSP00000356379.4:n.3742-54_3742-50delinsAGTAC
ENST00000680112.1:n.1798-54_1798-50delinsAGTAC
ENST00000680265.1:c.3742-54_3742-50delinsAGTAC ENSP00000505384.1:n.3742-54_3742-50delinsAGTAC
ENST00000680710.1:c.3742-54_3742-50delinsAGTAC ENSP00000506676.1:n.3742-54_3742-50delinsAGTAC
ENST00000681879.1:c.3742-54_3742-50delinsAGTAC ENSP00000505363.1:n.3742-54_3742-50delinsAGTAC
ENST00000294732.11:c.3742-54_3742-50delinsAGTAC ENSP00000294732.7:n.3742-54_3742-50delinsAGTAC
ENST00000367408.5:c.1492-54_1492-50delinsAGTAC ENSP00000356378.1:n.1492-54_1492-50delinsAGTAC
ENST00000367409.8:c.3742-54_3742-50delinsAGTAC ENSP00000356379.4:n.3742-54_3742-50delinsAGTAC
ENST00000612785.1:c.562-19450_562-19446delinsAGTAC ENSP00000479244.1:n.562-19450_562-19446delinsAGTAC
NM_001206846.1:c.3742-54_3742-50delinsAGTAC NP_001193775.1:n.3742-54_3742-50delinsAGTAC
NM_018136.4:c.3742-54_3742-50delinsAGTAC NP_060606.3:n.3742-54_3742-50delinsAGTAC
NM_018136.5:c.3742-54_3742-50delinsAGTAC MANE Select NP_060606.3:n.3742-54_3742-50delinsAGTAC
NM_001206846.2:c.3742-54_3742-50delinsAGTAC NP_001193775.1:n.3742-54_3742-50delinsAGTAC