Canonical Allele Identifier: CA645550295

Gene: ASB10

Linked Data

• COSMIC: COSM4448143

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187204_151187205delinsAA , CM000669.2:g.151187204_151187205delinsAA	GRCh38
NC_000007.13:g.150884291_150884292delinsAA , CM000669.1:g.150884291_150884292delinsAA	GRCh37
NC_000007.12:g.150515224_150515225delinsAA	NCBI36
NG_017016.1:g.5628_5629delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-75_-74delinsTT MANE Select	ENSP00000391137.2:n.-75_-74delinsTT
ENST00000275838.5:c.-75_-74delinsTT	ENSP00000275838.1:n.-75_-74delinsTT
ENST00000377867.7:c.271+247_271+248delinsTT	ENSP00000367098.3:n.271+247_271+248delinsTT
ENST00000415615.1:c.*121+49_*121+50delinsTT	ENSP00000410871.1:n.*121+49_*121+50delinsTT
NM_001142459.1:c.-75_-74delinsTT	NP_001135931.2:n.-75_-74delinsTT
NM_001142460.1:c.-75_-74delinsTT	NP_001135932.2:n.-75_-74delinsTT
NM_080871.3:c.271+247_271+248delinsTT	NP_543147.2:n.271+247_271+248delinsTT
XM_005249949.3:c.61_62delinsTT	XP_005250006.1:p.Pro21Phe
NM_001142459.2:c.-75_-74delinsTT MANE Select	NP_001135931.2:n.-75_-74delinsTT
NM_080871.4:c.271+247_271+248delinsTT	NP_543147.2:n.271+247_271+248delinsTT