Canonical Allele Identifier: CA2685657566

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186728-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186731del , CM000669.2:g.151186731del	GRCh38
NC_000007.13:g.150883818del , CM000669.1:g.150883818del	GRCh37
NC_000007.12:g.150514751del	NCBI36
NG_017016.1:g.6104del

Transcript Alleles

HGVS	Amino-acid change
ENST00000420175.3:c.317-70del MANE Select	ENSP00000391137.2:n.317-70del
ENST00000275838.5:c.317-70del	ENSP00000275838.1:n.317-70del
ENST00000377867.7:c.272-70del	ENSP00000367098.3:n.272-70del
ENST00000415615.1:c.*361-70del	ENSP00000410871.1:n.*361-70del
ENST00000420175.2:c.317-70del	ENSP00000391137.2:n.317-70del
NM_001142459.1:c.317-70del	NP_001135931.2:n.317-70del
NM_001142460.1:c.317-70del	NP_001135932.2:n.317-70del
NM_080871.3:c.272-70del	NP_543147.2:n.272-70del
XM_005249949.3:c.452-70del	XP_005250006.1:n.452-70del
NM_001142459.2:c.317-70del MANE Select	NP_001135931.2:n.317-70del
NM_080871.4:c.272-70del	NP_543147.2:n.272-70del