Canonical Allele Identifier: CA1217929797

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101084_197101087delinsTATA , CM000663.2:g.197101084_197101087delinsTATA	GRCh38
NC_000001.10:g.197070214_197070217delinsTATA , CM000663.1:g.197070214_197070217delinsTATA	GRCh37
NC_000001.9:g.195336837_195336840delinsTATA	NCBI36
NG_015867.1:g.50608_50611delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-4923_2108-4920delinsTATA
ENST00000367409.9:c.8164_8167delinsTATA MANE Select	ENSP00000356379.4:p.Tyr2722=
ENST00000680265.1:c.8164_8167delinsTATA	ENSP00000505384.1:p.Tyr2722=
ENST00000680710.1:c.8164_8167delinsTATA	ENSP00000506676.1:p.Tyr2722=
ENST00000294732.11:c.4066-4923_4066-4920delinsTATA	ENSP00000294732.7:n.4066-4923_4066-4920delinsTATA
ENST00000367408.5:c.1816-4923_1816-4920delinsTATA	ENSP00000356378.1:n.1816-4923_1816-4920delinsTATA
ENST00000367409.8:c.8164_8167delinsTATA	ENSP00000356379.4:p.Tyr2722=
ENST00000612785.1:c.2122_2125delinsTATA	ENSP00000479244.1:p.Tyr708=
NM_001206846.1:c.4066-4923_4066-4920delinsTATA	NP_001193775.1:n.4066-4923_4066-4920delinsTATA
NM_018136.4:c.8164_8167delinsTATA	NP_060606.3:p.Tyr2722=
NM_018136.5:c.8164_8167delinsTATA MANE Select	NP_060606.3:p.Tyr2722=
NM_001206846.2:c.4066-4923_4066-4920delinsTATA	NP_001193775.1:n.4066-4923_4066-4920delinsTATA