Canonical Allele Identifier: CA1752545567

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186837G= , CM000669.2:g.151186837G=	GRCh38
NC_000007.13:g.150883924G= , CM000669.1:g.150883924G=	GRCh37
NC_000007.12:g.150514857G=	NCBI36
NG_017016.1:g.5996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.294C= MANE Select	ENSP00000391137.2:p.Phe98=
ENST00000275838.5:c.294C=	ENSP00000275838.1:p.Phe98=
ENST00000377867.7:c.272-178C=	ENSP00000367098.3:n.272-178C=
ENST00000415615.1:c.*338C=	ENSP00000410871.1:n.*338C=
ENST00000420175.2:c.294C=	ENSP00000391137.2:p.Phe98=
NM_001142459.1:c.294C=	NP_001135931.2:p.Phe98=
NM_001142460.1:c.294C=	NP_001135932.2:p.Phe98=
NM_080871.3:c.272-178C=	NP_543147.2:n.272-178C=
XM_005249949.3:c.429C=	XP_005250006.1:p.Phe143=
NM_001142459.2:c.294C= MANE Select	NP_001135931.2:p.Phe98=
NM_080871.4:c.272-178C=	NP_543147.2:n.272-178C=