Canonical Allele Identifier: CA458881528

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884009_150884010del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186925_151186926del , CM000669.2:g.151186925_151186926del	GRCh38
NC_000007.13:g.150884012_150884013del , CM000669.1:g.150884012_150884013del	GRCh37
NC_000007.12:g.150514945_150514946del	NCBI36
NG_017016.1:g.5910_5911del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.208_209del MANE Select	ENSP00000391137.2:p.Val70LeufsTer14
ENST00000275838.5:c.208_209del	ENSP00000275838.1:p.Val70LeufsTer14
ENST00000377867.7:c.272-264_272-263del	ENSP00000367098.3:n.272-264_272-263del
ENST00000415615.1:c.*252_*253del	ENSP00000410871.1:n.*252_*253del
ENST00000420175.2:c.208_209del	ENSP00000391137.2:p.Val70LeufsTer14
NM_001142459.1:c.208_209del	NP_001135931.2:p.Val70LeufsTer14
NM_001142460.1:c.208_209del	NP_001135932.2:p.Val70LeufsTer14
NM_080871.3:c.272-264_272-263del	NP_543147.2:n.272-264_272-263del
XM_005249949.3:c.343_344del	XP_005250006.1:p.Val115LeufsTer14
NM_001142459.2:c.208_209del MANE Select	NP_001135931.2:p.Val70LeufsTer14
NM_080871.4:c.272-264_272-263del	NP_543147.2:n.272-264_272-263del