Canonical Allele Identifier: CA1217929781
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101049_197101051delinsGTT , CM000663.2:g.197101049_197101051delinsGTT GRCh38
NC_000001.10:g.197070179_197070181delinsGTT , CM000663.1:g.197070179_197070181delinsGTT GRCh37
NC_000001.9:g.195336802_195336804delinsGTT NCBI36
NG_015867.1:g.50644_50646delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-4887_2108-4885delinsAAC
ENST00000367409.9:c.8200_8202delinsAAC MANE Select ENSP00000356379.4:p.Asn2734=
ENST00000680265.1:c.8200_8202delinsAAC ENSP00000505384.1:p.Asn2734=
ENST00000680710.1:c.8200_8202delinsAAC ENSP00000506676.1:p.Asn2734=
ENST00000294732.11:c.4066-4887_4066-4885delinsAAC ENSP00000294732.7:n.4066-4887_4066-4885delinsAAC
ENST00000367408.5:c.1816-4887_1816-4885delinsAAC ENSP00000356378.1:n.1816-4887_1816-4885delinsAAC
ENST00000367409.8:c.8200_8202delinsAAC ENSP00000356379.4:p.Asn2734=
ENST00000612785.1:c.2158_2160delinsAAC ENSP00000479244.1:p.Asn720=
NM_001206846.1:c.4066-4887_4066-4885delinsAAC NP_001193775.1:n.4066-4887_4066-4885delinsAAC
NM_018136.4:c.8200_8202delinsAAC NP_060606.3:p.Asn2734=
NM_018136.5:c.8200_8202delinsAAC MANE Select NP_060606.3:p.Asn2734=
NM_001206846.2:c.4066-4887_4066-4885delinsAAC NP_001193775.1:n.4066-4887_4066-4885delinsAAC