Canonical Allele Identifier: CA1752545569

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186841T= , CM000669.2:g.151186841T=	GRCh38
NC_000007.13:g.150883928T= , CM000669.1:g.150883928T=	GRCh37
NC_000007.12:g.150514861T=	NCBI36
NG_017016.1:g.5992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.290A= MANE Select	ENSP00000391137.2:p.Asp97=
ENST00000275838.5:c.290A=	ENSP00000275838.1:p.Asp97=
ENST00000377867.7:c.272-182A=	ENSP00000367098.3:n.272-182A=
ENST00000415615.1:c.*334A=	ENSP00000410871.1:n.*334A=
ENST00000420175.2:c.290A=	ENSP00000391137.2:p.Asp97=
NM_001142459.1:c.290A=	NP_001135931.2:p.Asp97=
NM_001142460.1:c.290A=	NP_001135932.2:p.Asp97=
NM_080871.3:c.272-182A=	NP_543147.2:n.272-182A=
XM_005249949.3:c.425A=	XP_005250006.1:p.Asp142=
NM_001142459.2:c.290A= MANE Select	NP_001135931.2:p.Asp97=
NM_080871.4:c.272-182A=	NP_543147.2:n.272-182A=