Canonical Allele Identifier: CA579077282

Gene: ASB10

Linked Data

• dbSNP Id: rs1202115008
• gnomAD v2: 7-150884296-TACAG-T
• gnomAD v4: 7-151187209-TACAG-T
• MyVariant Identifiers: chr7:g.150884297_150884300del (hg19) ; chr7:g.151187210_151187213del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187219_151187222del , CM000669.2:g.151187219_151187222del	GRCh38
NC_000007.13:g.150884306_150884309del , CM000669.1:g.150884306_150884309del	GRCh37
NC_000007.12:g.150515239_150515242del	NCBI36
NG_017016.1:g.5620_5623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-83_-80del MANE Select	ENSP00000391137.2:n.-83_-80del
ENST00000275838.5:c.-83_-80del	ENSP00000275838.1:n.-83_-80del
ENST00000377867.7:c.271+239_271+242del	ENSP00000367098.3:n.271+239_271+242del
ENST00000415615.1:c.*121+41_*121+44del	ENSP00000410871.1:n.*121+41_*121+44del
NM_001142459.1:c.-83_-80del	NP_001135931.2:n.-83_-80del
NM_001142460.1:c.-83_-80del	NP_001135932.2:n.-83_-80del
NM_080871.3:c.271+239_271+242del	NP_543147.2:n.271+239_271+242del
XM_005249949.3:c.53_56del	XP_005250006.1:p.Ser18TyrfsTer30
NM_001142459.2:c.-83_-80del MANE Select	NP_001135931.2:n.-83_-80del
NM_080871.4:c.271+239_271+242del	NP_543147.2:n.271+239_271+242del