Canonical Allele Identifier: CA1752544727

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186372_151186374delinsTGG , CM000669.2:g.151186372_151186374delinsTGG	GRCh38
NC_000007.13:g.150883459_150883461delinsTGG , CM000669.1:g.150883459_150883461delinsTGG	GRCh37
NC_000007.12:g.150514392_150514394delinsTGG	NCBI36
NG_017016.1:g.6459_6461delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+18_584+20delinsCCA MANE Select	ENSP00000391137.2:n.584+18_584+20delinsCCA
ENST00000275838.5:c.584+18_584+20delinsCCA	ENSP00000275838.1:n.584+18_584+20delinsCCA
ENST00000377867.7:c.539+18_539+20delinsCCA	ENSP00000367098.3:n.539+18_539+20delinsCCA
ENST00000420175.2:c.584+18_584+20delinsCCA	ENSP00000391137.2:n.584+18_584+20delinsCCA
NM_001142459.1:c.584+18_584+20delinsCCA	NP_001135931.2:n.584+18_584+20delinsCCA
NM_001142460.1:c.584+18_584+20delinsCCA	NP_001135932.2:n.584+18_584+20delinsCCA
NM_080871.3:c.539+18_539+20delinsCCA	NP_543147.2:n.539+18_539+20delinsCCA
XM_005249949.3:c.719+18_719+20delinsCCA	XP_005250006.1:n.719+18_719+20delinsCCA
NM_001142459.2:c.584+18_584+20delinsCCA MANE Select	NP_001135931.2:n.584+18_584+20delinsCCA
NM_080871.4:c.539+18_539+20delinsCCA	NP_543147.2:n.539+18_539+20delinsCCA