Canonical Allele Identifier: CA1217946467

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143278_197143280delinsCTA , CM000663.2:g.197143278_197143280delinsCTA	GRCh38
NC_000001.10:g.197112408_197112410delinsCTA , CM000663.1:g.197112408_197112410delinsCTA	GRCh37
NC_000001.9:g.195379031_195379033delinsCTA	NCBI36
NG_015867.1:g.8415_8417delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.972_974delinsTAG MANE Select	ENSP00000356379.4:p.Asn324=
ENST00000679766.1:n.1189_1191delinsTAG
ENST00000680265.1:c.972_974delinsTAG	ENSP00000505384.1:p.Asn324=
ENST00000680710.1:c.972_974delinsTAG	ENSP00000506676.1:p.Asn324=
ENST00000681879.1:c.972_974delinsTAG	ENSP00000505363.1:p.Asn324=
ENST00000294732.11:c.972_974delinsTAG	ENSP00000294732.7:p.Asn324=
ENST00000367409.8:c.972_974delinsTAG	ENSP00000356379.4:p.Asn324=
ENST00000612785.1:c.561+411_561+413delinsTAG	ENSP00000479244.1:n.561+411_561+413delinsTAG
NM_001206846.1:c.972_974delinsTAG	NP_001193775.1:p.Asn324=
NM_018136.4:c.972_974delinsTAG	NP_060606.3:p.Asn324=
NM_018136.5:c.972_974delinsTAG MANE Select	NP_060606.3:p.Asn324=
NM_001206846.2:c.972_974delinsTAG	NP_001193775.1:p.Asn324=