Canonical Allele Identifier: CA645550294

Gene: ASB10

Linked Data

• COSMIC: COSM4517740 ; COSM4517741 ; COSM4517742

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187090_151187091delinsTT , CM000669.2:g.151187090_151187091delinsTT	GRCh38
NC_000007.13:g.150884177_150884178delinsTT , CM000669.1:g.150884177_150884178delinsTT	GRCh37
NC_000007.12:g.150515110_150515111delinsTT	NCBI36
NG_017016.1:g.5742_5743delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.40_41delinsAA MANE Select	ENSP00000391137.2:p.Gly14Lys
ENST00000275838.5:c.40_41delinsAA	ENSP00000275838.1:p.Gly14Lys
ENST00000377867.7:c.271+361_271+362delinsAA	ENSP00000367098.3:n.271+361_271+362delinsAA
ENST00000415615.1:c.*122-38_*122-37delinsAA	ENSP00000410871.1:n.*122-38_*122-37delinsAA
ENST00000420175.2:c.40_41delinsAA	ENSP00000391137.2:p.Gly14Lys
NM_001142459.1:c.40_41delinsAA	NP_001135931.2:p.Gly14Lys
NM_001142460.1:c.40_41delinsAA	NP_001135932.2:p.Gly14Lys
NM_080871.3:c.271+361_271+362delinsAA	NP_543147.2:n.271+361_271+362delinsAA
XM_005249949.3:c.175_176delinsAA	XP_005250006.1:p.Gly59Lys
NM_001142459.2:c.40_41delinsAA MANE Select	NP_001135931.2:p.Gly14Lys
NM_080871.4:c.271+361_271+362delinsAA	NP_543147.2:n.271+361_271+362delinsAA