Canonical Allele Identifier: CA2579066549

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186322_151186324del , CM000669.2:g.151186322_151186324del	GRCh38
NC_000007.13:g.150883409_150883411del , CM000669.1:g.150883409_150883411del	GRCh37
NC_000007.12:g.150514342_150514344del	NCBI36
NG_017016.1:g.6510_6512del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+69_584+71del MANE Select	ENSP00000391137.2:n.584+69_584+71del
ENST00000275838.5:c.584+69_584+71del	ENSP00000275838.1:n.584+69_584+71del
ENST00000377867.7:c.539+69_539+71del	ENSP00000367098.3:n.539+69_539+71del
ENST00000420175.2:c.584+69_584+71del	ENSP00000391137.2:n.584+69_584+71del
NM_001142459.1:c.584+69_584+71del	NP_001135931.2:n.584+69_584+71del
NM_001142460.1:c.584+69_584+71del	NP_001135932.2:n.584+69_584+71del
NM_080871.3:c.539+69_539+71del	NP_543147.2:n.539+69_539+71del
XM_005249949.3:c.719+69_719+71del	XP_005250006.1:n.719+69_719+71del
NM_001142459.2:c.584+69_584+71del MANE Select	NP_001135931.2:n.584+69_584+71del
NM_080871.4:c.539+69_539+71del	NP_543147.2:n.539+69_539+71del