Canonical Allele Identifier: CA1752544847

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186433C= , CM000669.2:g.151186433C=	GRCh38
NC_000007.13:g.150883520C= , CM000669.1:g.150883520C=	GRCh37
NC_000007.12:g.150514453C=	NCBI36
NG_017016.1:g.6400G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.543G= MANE Select	ENSP00000391137.2:p.Gly181=
ENST00000275838.5:c.543G=	ENSP00000275838.1:p.Gly181=
ENST00000377867.7:c.498G=	ENSP00000367098.3:p.Gly166=
ENST00000420175.2:c.543G=	ENSP00000391137.2:p.Gly181=
NM_001142459.1:c.543G=	NP_001135931.2:p.Gly181=
NM_001142460.1:c.543G=	NP_001135932.2:p.Gly181=
NM_080871.3:c.498G=	NP_543147.2:p.Gly166=
XM_005249949.3:c.678G=	XP_005250006.1:p.Gly226=
NM_001142459.2:c.543G= MANE Select	NP_001135931.2:p.Gly181=
NM_080871.4:c.498G=	NP_543147.2:p.Gly166=