Canonical Allele Identifier: CA1752545451

Gene: ASB10

Linked Data

• dbSNP Id: rs1801603005
• gnomAD v3: 7-151186738-C-G
• gnomAD v4: 7-151186738-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186738C>G , CM000669.2:g.151186738C>G	GRCh38
NC_000007.13:g.150883825C>G , CM000669.1:g.150883825C>G	GRCh37
NC_000007.12:g.150514758C>G	NCBI36
NG_017016.1:g.6095G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+77G>C MANE Select	ENSP00000391137.2:n.316+77G>C
ENST00000275838.5:c.316+77G>C	ENSP00000275838.1:n.316+77G>C
ENST00000377867.7:c.272-79G>C	ENSP00000367098.3:n.272-79G>C
ENST00000415615.1:c.*360+77G>C	ENSP00000410871.1:n.*360+77G>C
ENST00000420175.2:c.316+77G>C	ENSP00000391137.2:n.316+77G>C
NM_001142459.1:c.316+77G>C	NP_001135931.2:n.316+77G>C
NM_001142460.1:c.316+77G>C	NP_001135932.2:n.316+77G>C
NM_080871.3:c.272-79G>C	NP_543147.2:n.272-79G>C
XM_005249949.3:c.451+77G>C	XP_005250006.1:n.451+77G>C
NM_001142459.2:c.316+77G>C MANE Select	NP_001135931.2:n.316+77G>C
NM_080871.4:c.272-79G>C	NP_543147.2:n.272-79G>C