Canonical Allele Identifier: CA835247308

Gene: ASB10

Linked Data

• dbSNP Id: rs1409781573
• gnomAD v4: 7-151187130-TG-T
• MyVariant Identifiers: chr7:g.150884218del (hg19) ; chr7:g.151187131del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187131del , CM000669.2:g.151187131del	GRCh38
NC_000007.13:g.150884218del , CM000669.1:g.150884218del	GRCh37
NC_000007.12:g.150515151del	NCBI36
NG_017016.1:g.5702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-1del MANE Select	ENSP00000391137.2:n.-1del
ENST00000275838.5:c.-1del	ENSP00000275838.1:n.-1del
ENST00000377867.7:c.271+321del	ENSP00000367098.3:n.271+321del
ENST00000415615.1:c.*122-78del	ENSP00000410871.1:n.*122-78del
ENST00000420175.2:c.-1del	ENSP00000391137.2:n.-1del
NM_001142459.1:c.-1del	NP_001135931.2:n.-1del
NM_001142460.1:c.-1del	NP_001135932.2:n.-1del
NM_080871.3:c.271+321del	NP_543147.2:n.271+321del
XM_005249949.3:c.135del	XP_005250006.1:p.His45GlnfsTer4
NM_001142459.2:c.-1del MANE Select	NP_001135931.2:n.-1del
NM_080871.4:c.271+321del	NP_543147.2:n.271+321del