Canonical Allele Identifier: CA2685657773

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187353-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187353A>C , CM000669.2:g.151187353A>C	GRCh38
NC_000007.13:g.150884440A>C , CM000669.1:g.150884440A>C	GRCh37
NC_000007.12:g.150515373A>C	NCBI36
NG_017016.1:g.5480T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-223T>G	ENSP00000275838.1:n.-223T>G
ENST00000377867.7:c.271+99T>G	ENSP00000367098.3:n.271+99T>G
ENST00000415615.1:c.*22T>G	ENSP00000410871.1:n.*22T>G
NM_001142459.1:c.-223T>G	NP_001135931.2:n.-223T>G
NM_001142460.1:c.-223T>G	NP_001135932.2:n.-223T>G
NM_080871.3:c.271+99T>G	NP_543147.2:n.271+99T>G
NM_080871.4:c.271+99T>G	NP_543147.2:n.271+99T>G