Canonical Allele Identifier: CA645547260

Gene: ASB10

Linked Data

• COSMIC: COSM4565935 ; COSM4565936 ; COSM4565937

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186856_151186857delinsAA , CM000669.2:g.151186856_151186857delinsAA	GRCh38
NC_000007.13:g.150883943_150883944delinsAA , CM000669.1:g.150883943_150883944delinsAA	GRCh37
NC_000007.12:g.150514876_150514877delinsAA	NCBI36
NG_017016.1:g.5976_5977delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.274_275delinsTT MANE Select	ENSP00000391137.2:p.Pro92Leu
ENST00000275838.5:c.274_275delinsTT	ENSP00000275838.1:p.Pro92Leu
ENST00000377867.7:c.272-198_272-197delinsTT	ENSP00000367098.3:n.272-198_272-197delinsTT
ENST00000415615.1:c.*318_*319delinsTT	ENSP00000410871.1:n.*318_*319delinsTT
ENST00000420175.2:c.274_275delinsTT	ENSP00000391137.2:p.Pro92Leu
NM_001142459.1:c.274_275delinsTT	NP_001135931.2:p.Pro92Leu
NM_001142460.1:c.274_275delinsTT	NP_001135932.2:p.Pro92Leu
NM_080871.3:c.272-198_272-197delinsTT	NP_543147.2:n.272-198_272-197delinsTT
XM_005249949.3:c.409_410delinsTT	XP_005250006.1:p.Pro137Leu
NM_001142459.2:c.274_275delinsTT MANE Select	NP_001135931.2:p.Pro92Leu
NM_080871.4:c.272-198_272-197delinsTT	NP_543147.2:n.272-198_272-197delinsTT