Canonical Allele Identifier: CA169126163

Gene: ASB10

Linked Data

• dbSNP Id: rs1027713259
• gnomAD v2: 7-150884172-GC-G
• gnomAD v3: 7-151187085-GC-G
• gnomAD v4: 7-151187085-GC-G
• MyVariant Identifiers: chr7:g.150884173del (hg19) ; chr7:g.151187086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187086del , CM000669.2:g.151187086del	GRCh38
NC_000007.13:g.150884173del , CM000669.1:g.150884173del	GRCh37
NC_000007.12:g.150515106del	NCBI36
NG_017016.1:g.5747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.45del MANE Select	ENSP00000391137.2:p.Glu15AspfsTer?
ENST00000275838.5:c.45del	ENSP00000275838.1:p.Glu15AspfsTer?
ENST00000377867.7:c.271+366del	ENSP00000367098.3:n.271+366del
ENST00000415615.1:c.*122-33del	ENSP00000410871.1:n.*122-33del
ENST00000420175.2:c.45del	ENSP00000391137.2:p.Glu15AspfsTer?
NM_001142459.1:c.45del	NP_001135931.2:p.Glu15AspfsTer?
NM_001142460.1:c.45del	NP_001135932.2:p.Glu15AspfsTer?
NM_080871.3:c.271+366del	NP_543147.2:n.271+366del
XM_005249949.3:c.180del	XP_005250006.1:p.Glu60AspfsTer?
NM_001142459.2:c.45del MANE Select	NP_001135931.2:p.Glu15AspfsTer?
NM_080871.4:c.271+366del	NP_543147.2:n.271+366del