Canonical Allele Identifier: CA579077283

Gene: ASB10

Linked Data

• dbSNP Id: rs1244988197
• gnomAD v2: 7-150884322-CCCACGCT-C
• gnomAD v4: 7-151187235-CCCACGCT-C
• MyVariant Identifiers: chr7:g.150884323_150884329del (hg19) ; chr7:g.151187236_151187242del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187238_151187244del , CM000669.2:g.151187238_151187244del	GRCh38
NC_000007.13:g.150884325_150884331del , CM000669.1:g.150884325_150884331del	GRCh37
NC_000007.12:g.150515258_150515264del	NCBI36
NG_017016.1:g.5591_5597del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-112_-106del MANE Select	ENSP00000391137.2:n.-112_-106del
ENST00000275838.5:c.-112_-106del	ENSP00000275838.1:n.-112_-106del
ENST00000377867.7:c.271+210_271+216del	ENSP00000367098.3:n.271+210_271+216del
ENST00000415615.1:c.*121+12_*121+18del	ENSP00000410871.1:n.*121+12_*121+18del
NM_001142459.1:c.-112_-106del	NP_001135931.2:n.-112_-106del
NM_001142460.1:c.-112_-106del	NP_001135932.2:n.-112_-106del
NM_080871.3:c.271+210_271+216del	NP_543147.2:n.271+210_271+216del
XM_005249949.3:c.24_30del	XP_005250006.1:p.Ala9ThrfsTer?
NM_001142459.2:c.-112_-106del MANE Select	NP_001135931.2:n.-112_-106del
NM_080871.4:c.271+210_271+216del	NP_543147.2:n.271+210_271+216del