Canonical Allele Identifier: CA1217945905

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142880_197142882delinsTCA , CM000663.2:g.197142880_197142882delinsTCA	GRCh38
NC_000001.10:g.197112010_197112012delinsTCA , CM000663.1:g.197112010_197112012delinsTCA	GRCh37
NC_000001.9:g.195378633_195378635delinsTCA	NCBI36
NG_015867.1:g.8813_8815delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1370_1372delinsTGA MANE Select	ENSP00000356379.4:p.Met457=
ENST00000679766.1:n.1587_1589delinsTGA
ENST00000680265.1:c.1370_1372delinsTGA	ENSP00000505384.1:p.Met457=
ENST00000680710.1:c.1370_1372delinsTGA	ENSP00000506676.1:p.Met457=
ENST00000681879.1:c.1370_1372delinsTGA	ENSP00000505363.1:p.Met457=
ENST00000294732.11:c.1370_1372delinsTGA	ENSP00000294732.7:p.Met457=
ENST00000367409.8:c.1370_1372delinsTGA	ENSP00000356379.4:p.Met457=
ENST00000612785.1:c.561+809_561+811delinsTGA	ENSP00000479244.1:n.561+809_561+811delinsTGA
NM_001206846.1:c.1370_1372delinsTGA	NP_001193775.1:p.Met457=
NM_018136.4:c.1370_1372delinsTGA	NP_060606.3:p.Met457=
NM_018136.5:c.1370_1372delinsTGA MANE Select	NP_060606.3:p.Met457=
NM_001206846.2:c.1370_1372delinsTGA	NP_001193775.1:p.Met457=