Canonical Allele Identifier: CA1752544623

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186265_151186267delinsCCT , CM000669.2:g.151186265_151186267delinsCCT	GRCh38
NC_000007.13:g.150883352_150883354delinsCCT , CM000669.1:g.150883352_150883354delinsCCT	GRCh37
NC_000007.12:g.150514285_150514287delinsCCT	NCBI36
NG_017016.1:g.6566_6568delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+125_584+127delinsAGG MANE Select	ENSP00000391137.2:n.584+125_584+127delinsAGG
ENST00000275838.5:c.584+125_584+127delinsAGG	ENSP00000275838.1:n.584+125_584+127delinsAGG
ENST00000377867.7:c.539+125_539+127delinsAGG	ENSP00000367098.3:n.539+125_539+127delinsAGG
ENST00000420175.2:c.584+125_584+127delinsAGG	ENSP00000391137.2:n.584+125_584+127delinsAGG
NM_001142459.1:c.584+125_584+127delinsAGG	NP_001135931.2:n.584+125_584+127delinsAGG
NM_001142460.1:c.584+125_584+127delinsAGG	NP_001135932.2:n.584+125_584+127delinsAGG
NM_080871.3:c.539+125_539+127delinsAGG	NP_543147.2:n.539+125_539+127delinsAGG
XM_005249949.3:c.719+125_719+127delinsAGG	XP_005250006.1:n.719+125_719+127delinsAGG
NM_001142459.2:c.584+125_584+127delinsAGG MANE Select	NP_001135931.2:n.584+125_584+127delinsAGG
NM_080871.4:c.539+125_539+127delinsAGG	NP_543147.2:n.539+125_539+127delinsAGG