Canonical Allele Identifier: CA1217938466
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197122053_197122054delinsAC , CM000663.2:g.197122053_197122054delinsAC GRCh38
NC_000001.10:g.197091183_197091184delinsAC , CM000663.1:g.197091183_197091184delinsAC GRCh37
NC_000001.9:g.195357806_195357807delinsAC NCBI36
NG_015867.1:g.29641_29642delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1784-11_1784-10delinsGT
ENST00000367409.9:c.3742-11_3742-10delinsGT MANE Select ENSP00000356379.4:n.3742-11_3742-10delinsGT
ENST00000680112.1:n.1798-11_1798-10delinsGT
ENST00000680265.1:c.3742-11_3742-10delinsGT ENSP00000505384.1:n.3742-11_3742-10delinsGT
ENST00000680710.1:c.3742-11_3742-10delinsGT ENSP00000506676.1:n.3742-11_3742-10delinsGT
ENST00000681879.1:c.3742-11_3742-10delinsGT ENSP00000505363.1:n.3742-11_3742-10delinsGT
ENST00000294732.11:c.3742-11_3742-10delinsGT ENSP00000294732.7:n.3742-11_3742-10delinsGT
ENST00000367408.5:c.1492-11_1492-10delinsGT ENSP00000356378.1:n.1492-11_1492-10delinsGT
ENST00000367409.8:c.3742-11_3742-10delinsGT ENSP00000356379.4:n.3742-11_3742-10delinsGT
ENST00000612785.1:c.562-19407_562-19406delinsGT ENSP00000479244.1:n.562-19407_562-19406delinsGT
NM_001206846.1:c.3742-11_3742-10delinsGT NP_001193775.1:n.3742-11_3742-10delinsGT
NM_018136.4:c.3742-11_3742-10delinsGT NP_060606.3:n.3742-11_3742-10delinsGT
NM_018136.5:c.3742-11_3742-10delinsGT MANE Select NP_060606.3:n.3742-11_3742-10delinsGT
NM_001206846.2:c.3742-11_3742-10delinsGT NP_001193775.1:n.3742-11_3742-10delinsGT