Canonical Allele Identifier: CA1752545124

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186551_151186563delinsGGCCTTGCTCGCC , CM000669.2:g.151186551_151186563delinsGGCCTTGCTCGCC	GRCh38
NC_000007.13:g.150883638_150883650delinsGGCCTTGCTCGCC , CM000669.1:g.150883638_150883650delinsGGCCTTGCTCGCC	GRCh37
NC_000007.12:g.150514571_150514583delinsGGCCTTGCTCGCC	NCBI36
NG_017016.1:g.6270_6282delinsGGCGAGCAAGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.413_425delinsGGCGAGCAAGGCC MANE Select	ENSP00000391137.2:p.Arg138=
ENST00000275838.5:c.413_425delinsGGCGAGCAAGGCC	ENSP00000275838.1:p.Arg138=
ENST00000377867.7:c.368_380delinsGGCGAGCAAGGCC	ENSP00000367098.3:p.Arg123=
ENST00000420175.2:c.413_425delinsGGCGAGCAAGGCC	ENSP00000391137.2:p.Arg138=
NM_001142459.1:c.413_425delinsGGCGAGCAAGGCC	NP_001135931.2:p.Arg138=
NM_001142460.1:c.413_425delinsGGCGAGCAAGGCC	NP_001135932.2:p.Arg138=
NM_080871.3:c.368_380delinsGGCGAGCAAGGCC	NP_543147.2:p.Arg123=
XM_005249949.3:c.548_560delinsGGCGAGCAAGGCC	XP_005250006.1:p.Arg183=
NM_001142459.2:c.413_425delinsGGCGAGCAAGGCC MANE Select	NP_001135931.2:p.Arg138=
NM_080871.4:c.368_380delinsGGCGAGCAAGGCC	NP_543147.2:p.Arg123=