Canonical Allele Identifier: CA2685657684

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187196-A-AGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187197_151187198insAGGG , CM000669.2:g.151187197_151187198insAGGG	GRCh38
NC_000007.13:g.150884284_150884285insAGGG , CM000669.1:g.150884284_150884285insAGGG	GRCh37
NC_000007.12:g.150515217_150515218insAGGG	NCBI36
NG_017016.1:g.5636_5637insCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-67_-66insCCTC MANE Select	ENSP00000391137.2:n.-67_-66insCCTC
ENST00000275838.5:c.-67_-66insCCTC	ENSP00000275838.1:n.-67_-66insCCTC
ENST00000377867.7:c.271+255_271+256insCCTC	ENSP00000367098.3:n.271+255_271+256insCCTC
ENST00000415615.1:c.*121+57_*121+58insCCTC	ENSP00000410871.1:n.*121+57_*121+58insCCTC
NM_001142459.1:c.-67_-66insCCTC	NP_001135931.2:n.-67_-66insCCTC
NM_001142460.1:c.-67_-66insCCTC	NP_001135932.2:n.-67_-66insCCTC
NM_080871.3:c.271+255_271+256insCCTC	NP_543147.2:n.271+255_271+256insCCTC
XM_005249949.3:c.69_70insCCTC	XP_005250006.1:p.Ser24ProfsTer?
NM_001142459.2:c.-67_-66insCCTC MANE Select	NP_001135931.2:n.-67_-66insCCTC
NM_080871.4:c.271+255_271+256insCCTC	NP_543147.2:n.271+255_271+256insCCTC