Canonical Allele Identifier: CA1217946059

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142995_197142996delinsAT , CM000663.2:g.197142995_197142996delinsAT	GRCh38
NC_000001.10:g.197112125_197112126delinsAT , CM000663.1:g.197112125_197112126delinsAT	GRCh37
NC_000001.9:g.195378748_195378749delinsAT	NCBI36
NG_015867.1:g.8699_8700delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367409.9:c.1256_1257delinsAT MANE Select	ENSP00000356379.4:p.Asn419=
ENST00000679766.1:n.1473_1474delinsAT
ENST00000680265.1:c.1256_1257delinsAT	ENSP00000505384.1:p.Asn419=
ENST00000680710.1:c.1256_1257delinsAT	ENSP00000506676.1:p.Asn419=
ENST00000681879.1:c.1256_1257delinsAT	ENSP00000505363.1:p.Asn419=
ENST00000294732.11:c.1256_1257delinsAT	ENSP00000294732.7:p.Asn419=
ENST00000367409.8:c.1256_1257delinsAT	ENSP00000356379.4:p.Asn419=
ENST00000612785.1:c.561+695_561+696delinsAT	ENSP00000479244.1:n.561+695_561+696delins...
NM_001206846.1:c.1256_1257delinsAT	NP_001193775.1:p.Asn419=
NM_018136.4:c.1256_1257delinsAT	NP_060606.3:p.Asn419=
NM_018136.5:c.1256_1257delinsAT MANE Select	NP_060606.3:p.Asn419=
NM_001206846.2:c.1256_1257delinsAT	NP_001193775.1:p.Asn419=