Canonical Allele Identifier: CA2685657679

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187191-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187192_151187193insCA , CM000669.2:g.151187192_151187193insCA	GRCh38
NC_000007.13:g.150884279_150884280insCA , CM000669.1:g.150884279_150884280insCA	GRCh37
NC_000007.12:g.150515212_150515213insCA	NCBI36
NG_017016.1:g.5641_5642insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-62_-61insGT MANE Select	ENSP00000391137.2:n.-62_-61insGT
ENST00000275838.5:c.-62_-61insGT	ENSP00000275838.1:n.-62_-61insGT
ENST00000377867.7:c.271+260_271+261insGT	ENSP00000367098.3:n.271+260_271+261insGT
ENST00000415615.1:c.*121+62_*121+63insGT	ENSP00000410871.1:n.*121+62_*121+63insGT
NM_001142459.1:c.-62_-61insGT	NP_001135931.2:n.-62_-61insGT
NM_001142460.1:c.-62_-61insGT	NP_001135932.2:n.-62_-61insGT
NM_080871.3:c.271+260_271+261insGT	NP_543147.2:n.271+260_271+261insGT
XM_005249949.3:c.74_75insGT	XP_005250006.1:p.Pro30CysfsTer20
NM_001142459.2:c.-62_-61insGT MANE Select	NP_001135931.2:n.-62_-61insGT
NM_080871.4:c.271+260_271+261insGT	NP_543147.2:n.271+260_271+261insGT