Canonical Allele Identifier: CA1752544866

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186447C= , CM000669.2:g.151186447C=	GRCh38
NC_000007.13:g.150883534C= , CM000669.1:g.150883534C=	GRCh37
NC_000007.12:g.150514467C=	NCBI36
NG_017016.1:g.6386G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.529G= MANE Select	ENSP00000391137.2:p.Ala177=
ENST00000275838.5:c.529G=	ENSP00000275838.1:p.Ala177=
ENST00000377867.7:c.484G=	ENSP00000367098.3:p.Ala162=
ENST00000420175.2:c.529G=	ENSP00000391137.2:p.Ala177=
NM_001142459.1:c.529G=	NP_001135931.2:p.Ala177=
NM_001142460.1:c.529G=	NP_001135932.2:p.Ala177=
NM_080871.3:c.484G=	NP_543147.2:p.Ala162=
XM_005249949.3:c.664G=	XP_005250006.1:p.Ala222=
NM_001142459.2:c.529G= MANE Select	NP_001135931.2:p.Ala177=
NM_080871.4:c.484G=	NP_543147.2:p.Ala162=