Canonical Allele Identifier: CA1752545518

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186786C= , CM000669.2:g.151186786C=	GRCh38
NC_000007.13:g.150883873C= , CM000669.1:g.150883873C=	GRCh37
NC_000007.12:g.150514806C=	NCBI36
NG_017016.1:g.6047G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+29G= MANE Select	ENSP00000391137.2:n.316+29G=
ENST00000275838.5:c.316+29G=	ENSP00000275838.1:n.316+29G=
ENST00000377867.7:c.272-127G=	ENSP00000367098.3:n.272-127G=
ENST00000415615.1:c.*360+29G=	ENSP00000410871.1:n.*360+29G=
ENST00000420175.2:c.316+29G=	ENSP00000391137.2:n.316+29G=
NM_001142459.1:c.316+29G=	NP_001135931.2:n.316+29G=
NM_001142460.1:c.316+29G=	NP_001135932.2:n.316+29G=
NM_080871.3:c.272-127G=	NP_543147.2:n.272-127G=
XM_005249949.3:c.451+29G=	XP_005250006.1:n.451+29G=
NM_001142459.2:c.316+29G= MANE Select	NP_001135931.2:n.316+29G=
NM_080871.4:c.272-127G=	NP_543147.2:n.272-127G=