Canonical Allele Identifier: CA2685657609

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186787-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186787T>G , CM000669.2:g.151186787T>G	GRCh38
NC_000007.13:g.150883874T>G , CM000669.1:g.150883874T>G	GRCh37
NC_000007.12:g.150514807T>G	NCBI36
NG_017016.1:g.6046A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+28A>C MANE Select	ENSP00000391137.2:n.316+28A>C
ENST00000275838.5:c.316+28A>C	ENSP00000275838.1:n.316+28A>C
ENST00000377867.7:c.272-128A>C	ENSP00000367098.3:n.272-128A>C
ENST00000415615.1:c.*360+28A>C	ENSP00000410871.1:n.*360+28A>C
ENST00000420175.2:c.316+28A>C	ENSP00000391137.2:n.316+28A>C
NM_001142459.1:c.316+28A>C	NP_001135931.2:n.316+28A>C
NM_001142460.1:c.316+28A>C	NP_001135932.2:n.316+28A>C
NM_080871.3:c.272-128A>C	NP_543147.2:n.272-128A>C
XM_005249949.3:c.451+28A>C	XP_005250006.1:n.451+28A>C
NM_001142459.2:c.316+28A>C MANE Select	NP_001135931.2:n.316+28A>C
NM_080871.4:c.272-128A>C	NP_543147.2:n.272-128A>C