Canonical Allele Identifier: CA1752544624

Gene: ASB10

Linked Data

• dbSNP Id: rs1801586892
• gnomAD v4: 7-151186265-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186266_151186267del , CM000669.2:g.151186266_151186267del	GRCh38
NC_000007.13:g.150883353_150883354del , CM000669.1:g.150883353_150883354del	GRCh37
NC_000007.12:g.150514286_150514287del	NCBI36
NG_017016.1:g.6566_6567del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+125_584+126del MANE Select	ENSP00000391137.2:n.584+125_584+126del
ENST00000275838.5:c.584+125_584+126del	ENSP00000275838.1:n.584+125_584+126del
ENST00000377867.7:c.539+125_539+126del	ENSP00000367098.3:n.539+125_539+126del
ENST00000420175.2:c.584+125_584+126del	ENSP00000391137.2:n.584+125_584+126del
NM_001142459.1:c.584+125_584+126del	NP_001135931.2:n.584+125_584+126del
NM_001142460.1:c.584+125_584+126del	NP_001135932.2:n.584+125_584+126del
NM_080871.3:c.539+125_539+126del	NP_543147.2:n.539+125_539+126del
XM_005249949.3:c.719+125_719+126del	XP_005250006.1:n.719+125_719+126del
NM_001142459.2:c.584+125_584+126del MANE Select	NP_001135931.2:n.584+125_584+126del
NM_080871.4:c.539+125_539+126del	NP_543147.2:n.539+125_539+126del