Canonical Allele Identifier: CA169126348

Gene: ASB10

Linked Data

• dbSNP Id: rs757365656
• gnomAD v2: 7-150884284-GC-G
• gnomAD v4: 7-151187197-GC-G
• MyVariant Identifiers: chr7:g.150884285del (hg19) ; chr7:g.151187198del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187198del , CM000669.2:g.151187198del	GRCh38
NC_000007.13:g.150884285del , CM000669.1:g.150884285del	GRCh37
NC_000007.12:g.150515218del	NCBI36
NG_017016.1:g.5635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-68del MANE Select	ENSP00000391137.2:n.-68del
ENST00000275838.5:c.-68del	ENSP00000275838.1:n.-68del
ENST00000377867.7:c.271+254del	ENSP00000367098.3:n.271+254del
ENST00000415615.1:c.*121+56del	ENSP00000410871.1:n.*121+56del
NM_001142459.1:c.-68del	NP_001135931.2:n.-68del
NM_001142460.1:c.-68del	NP_001135932.2:n.-68del
NM_080871.3:c.271+254del	NP_543147.2:n.271+254del
XM_005249949.3:c.68del	XP_005250006.1:p.Cys23SerfsTer26
NM_001142459.2:c.-68del MANE Select	NP_001135931.2:n.-68del
NM_080871.4:c.271+254del	NP_543147.2:n.271+254del