Canonical Allele Identifier: CA1752546063

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187199_151187200delinsAG , CM000669.2:g.151187199_151187200delinsAG	GRCh38
NC_000007.13:g.150884286_150884287delinsAG , CM000669.1:g.150884286_150884287delinsAG	GRCh37
NC_000007.12:g.150515219_150515220delinsAG	NCBI36
NG_017016.1:g.5633_5634delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-70_-69delinsCT MANE Select	ENSP00000391137.2:n.-70_-69delinsCT
ENST00000275838.5:c.-70_-69delinsCT	ENSP00000275838.1:n.-70_-69delinsCT
ENST00000377867.7:c.271+252_271+253delinsCT	ENSP00000367098.3:n.271+252_271+253delinsCT
ENST00000415615.1:c.*121+54_*121+55delinsCT	ENSP00000410871.1:n.*121+54_*121+55delinsCT
NM_001142459.1:c.-70_-69delinsCT	NP_001135931.2:n.-70_-69delinsCT
NM_001142460.1:c.-70_-69delinsCT	NP_001135932.2:n.-70_-69delinsCT
NM_080871.3:c.271+252_271+253delinsCT	NP_543147.2:n.271+252_271+253delinsCT
XM_005249949.3:c.66_67delinsCT	XP_005250006.1:p.Ser22=
NM_001142459.2:c.-70_-69delinsCT MANE Select	NP_001135931.2:n.-70_-69delinsCT
NM_080871.4:c.271+252_271+253delinsCT	NP_543147.2:n.271+252_271+253delinsCT