Canonical Allele Identifier: CA1752545585

Gene: ASB10

Linked Data

• dbSNP Id: rs1801606939

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186871_151186872del , CM000669.2:g.151186871_151186872del	GRCh38
NC_000007.13:g.150883958_150883959del , CM000669.1:g.150883958_150883959del	GRCh37
NC_000007.12:g.150514891_150514892del	NCBI36
NG_017016.1:g.5962_5963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.260_261del MANE Select	ENSP00000391137.2:p.Phe87Ter
ENST00000275838.5:c.260_261del	ENSP00000275838.1:p.Phe87Ter
ENST00000377867.7:c.272-212_272-211del	ENSP00000367098.3:n.272-212_272-211del
ENST00000415615.1:c.*304_*305del	ENSP00000410871.1:n.*304_*305del
ENST00000420175.2:c.260_261del	ENSP00000391137.2:p.Phe87Ter
NM_001142459.1:c.260_261del	NP_001135931.2:p.Phe87Ter
NM_001142460.1:c.260_261del	NP_001135932.2:p.Phe87Ter
NM_080871.3:c.272-212_272-211del	NP_543147.2:n.272-212_272-211del
XM_005249949.3:c.395_396del	XP_005250006.1:p.Phe132Ter
NM_001142459.2:c.260_261del MANE Select	NP_001135931.2:p.Phe87Ter
NM_080871.4:c.272-212_272-211del	NP_543147.2:n.272-212_272-211del