Canonical Allele Identifier: CA1217923469

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088246_197088250delinsTAATA , CM000663.2:g.197088246_197088250delinsTAATA	GRCh38
NC_000001.10:g.197057376_197057380delinsTAATA , CM000663.1:g.197057376_197057380delinsTAATA	GRCh37
NC_000001.9:g.195323999_195324003delinsTAATA	NCBI36
NG_015867.1:g.63445_63449delinsTATTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3448+6_3448+10delinsTATTA
ENST00000367409.9:c.10161+6_10161+10delinsTATTA MANE Select	ENSP00000356379.4:n.10161+6_10161+10delinsTATTA
ENST00000680265.1:c.10383+6_10383+10delinsTATTA	ENSP00000505384.1:n.10383+6_10383+10delinsTATTA
ENST00000680710.1:c.10137+6_10137+10delinsTATTA	ENSP00000506676.1:n.10137+6_10137+10delinsTATTA
ENST00000294732.11:c.5406+6_5406+10delinsTATTA	ENSP00000294732.7:n.5406+6_5406+10delinsTATTA
ENST00000367408.5:c.3156+6_3156+10delinsTATTA	ENSP00000356378.1:n.3156+6_3156+10delinsTATTA
ENST00000367409.8:c.10161+6_10161+10delinsTATTA	ENSP00000356379.4:n.10161+6_10161+10delinsTATTA
ENST00000612785.1:c.4125_4129delinsTATTA	ENSP00000479244.1:p.Ser1375=
NM_001206846.1:c.5406+6_5406+10delinsTATTA	NP_001193775.1:n.5406+6_5406+10delinsTATTA
NM_018136.4:c.10161+6_10161+10delinsTATTA	NP_060606.3:n.10161+6_10161+10delinsTATTA
NM_018136.5:c.10161+6_10161+10delinsTATTA MANE Select	NP_060606.3:n.10161+6_10161+10delinsTATTA
NM_001206846.2:c.5406+6_5406+10delinsTATTA	NP_001193775.1:n.5406+6_5406+10delinsTATTA