Canonical Allele Identifier: CA1752544969

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186493A= , CM000669.2:g.151186493A=	GRCh38
NC_000007.13:g.150883580A= , CM000669.1:g.150883580A=	GRCh37
NC_000007.12:g.150514513A=	NCBI36
NG_017016.1:g.6340T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.483T= MANE Select	ENSP00000391137.2:p.Thr161=
ENST00000275838.5:c.483T=	ENSP00000275838.1:p.Thr161=
ENST00000377867.7:c.438T=	ENSP00000367098.3:p.Thr146=
ENST00000420175.2:c.483T=	ENSP00000391137.2:p.Thr161=
NM_001142459.1:c.483T=	NP_001135931.2:p.Thr161=
NM_001142460.1:c.483T=	NP_001135932.2:p.Thr161=
NM_080871.3:c.438T=	NP_543147.2:p.Thr146=
XM_005249949.3:c.618T=	XP_005250006.1:p.Thr206=
NM_001142459.2:c.483T= MANE Select	NP_001135931.2:p.Thr161=
NM_080871.4:c.438T=	NP_543147.2:p.Thr146=