Canonical Allele Identifier: CA579077196

Gene: ASB10

Linked Data

• gnomAD v2: 7-150883318-GT-G
• MyVariant Identifiers: chr7:g.150883319del (hg19) ; chr7:g.151186232del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186232del , CM000669.2:g.151186232del	GRCh38
NC_000007.13:g.150883319del , CM000669.1:g.150883319del	GRCh37
NC_000007.12:g.150514252del	NCBI36
NG_017016.1:g.6601del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+160del MANE Select	ENSP00000391137.2:n.584+160del
ENST00000275838.5:c.584+160del	ENSP00000275838.1:n.584+160del
ENST00000377867.7:c.539+160del	ENSP00000367098.3:n.539+160del
ENST00000420175.2:c.584+160del	ENSP00000391137.2:n.584+160del
NM_001142459.1:c.584+160del	NP_001135931.2:n.584+160del
NM_001142460.1:c.584+160del	NP_001135932.2:n.584+160del
NM_080871.3:c.539+160del	NP_543147.2:n.539+160del
XM_005249949.3:c.719+160del	XP_005250006.1:n.719+160del
NM_001142459.2:c.584+160del MANE Select	NP_001135931.2:n.584+160del
NM_080871.4:c.539+160del	NP_543147.2:n.539+160del