Canonical Allele Identifier: CA1752544842

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186430T= , CM000669.2:g.151186430T=	GRCh38
NC_000007.13:g.150883517T= , CM000669.1:g.150883517T=	GRCh37
NC_000007.12:g.150514450T=	NCBI36
NG_017016.1:g.6403A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.546A= MANE Select	ENSP00000391137.2:p.Lys182=
ENST00000275838.5:c.546A=	ENSP00000275838.1:p.Lys182=
ENST00000377867.7:c.501A=	ENSP00000367098.3:p.Lys167=
ENST00000420175.2:c.546A=	ENSP00000391137.2:p.Lys182=
NM_001142459.1:c.546A=	NP_001135931.2:p.Lys182=
NM_001142460.1:c.546A=	NP_001135932.2:p.Lys182=
NM_080871.3:c.501A=	NP_543147.2:p.Lys167=
XM_005249949.3:c.681A=	XP_005250006.1:p.Lys227=
NM_001142459.2:c.546A= MANE Select	NP_001135931.2:p.Lys182=
NM_080871.4:c.501A=	NP_543147.2:p.Lys167=