Canonical Allele Identifier: CA1752544713

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186366G= , CM000669.2:g.151186366G=	GRCh38
NC_000007.13:g.150883453G= , CM000669.1:g.150883453G=	GRCh37
NC_000007.12:g.150514386G=	NCBI36
NG_017016.1:g.6467C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000420175.3:c.584+26C= MANE Select	ENSP00000391137.2:n.584+26C=
ENST00000275838.5:c.584+26C=	ENSP00000275838.1:n.584+26C=
ENST00000377867.7:c.539+26C=	ENSP00000367098.3:n.539+26C=
ENST00000420175.2:c.584+26C=	ENSP00000391137.2:n.584+26C=
NM_001142459.1:c.584+26C=	NP_001135931.2:n.584+26C=
NM_001142460.1:c.584+26C=	NP_001135932.2:n.584+26C=
NM_080871.3:c.539+26C=	NP_543147.2:n.539+26C=
XM_005249949.3:c.719+26C=	XP_005250006.1:n.719+26C=
NM_001142459.2:c.584+26C= MANE Select	NP_001135931.2:n.584+26C=
NM_080871.4:c.539+26C=	NP_543147.2:n.539+26C=