Canonical Allele Identifier: CA1752544816

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186418A= , CM000669.2:g.151186418A=	GRCh38
NC_000007.13:g.150883505A= , CM000669.1:g.150883505A=	GRCh37
NC_000007.12:g.150514438A=	NCBI36
NG_017016.1:g.6415T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.558T= MANE Select	ENSP00000391137.2:p.His186=
ENST00000275838.5:c.558T=	ENSP00000275838.1:p.His186=
ENST00000377867.7:c.513T=	ENSP00000367098.3:p.His171=
ENST00000420175.2:c.558T=	ENSP00000391137.2:p.His186=
NM_001142459.1:c.558T=	NP_001135931.2:p.His186=
NM_001142460.1:c.558T=	NP_001135932.2:p.His186=
NM_080871.3:c.513T=	NP_543147.2:p.His171=
XM_005249949.3:c.693T=	XP_005250006.1:p.His231=
NM_001142459.2:c.558T= MANE Select	NP_001135931.2:p.His186=
NM_080871.4:c.513T=	NP_543147.2:p.His171=