Canonical Allele Identifier: CA1752544874

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186452T= , CM000669.2:g.151186452T=	GRCh38
NC_000007.13:g.150883539T= , CM000669.1:g.150883539T=	GRCh37
NC_000007.12:g.150514472T=	NCBI36
NG_017016.1:g.6381A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.524A= MANE Select	ENSP00000391137.2:p.Asn175=
ENST00000275838.5:c.524A=	ENSP00000275838.1:p.Asn175=
ENST00000377867.7:c.479A=	ENSP00000367098.3:p.Asn160=
ENST00000420175.2:c.524A=	ENSP00000391137.2:p.Asn175=
NM_001142459.1:c.524A=	NP_001135931.2:p.Asn175=
NM_001142460.1:c.524A=	NP_001135932.2:p.Asn175=
NM_080871.3:c.479A=	NP_543147.2:p.Asn160=
XM_005249949.3:c.659A=	XP_005250006.1:p.Asn220=
NM_001142459.2:c.524A= MANE Select	NP_001135931.2:p.Asn175=
NM_080871.4:c.479A=	NP_543147.2:p.Asn160=