Canonical Allele Identifier: CA1752545929

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187113A= , CM000669.2:g.151187113A=	GRCh38
NC_000007.13:g.150884200A= , CM000669.1:g.150884200A=	GRCh37
NC_000007.12:g.150515133A=	NCBI36
NG_017016.1:g.5720T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.18T= MANE Select	ENSP00000391137.2:p.Ser6=
ENST00000275838.5:c.18T=	ENSP00000275838.1:p.Ser6=
ENST00000377867.7:c.271+339T=	ENSP00000367098.3:n.271+339T=
ENST00000415615.1:c.*122-60T=	ENSP00000410871.1:n.*122-60T=
ENST00000420175.2:c.18T=	ENSP00000391137.2:p.Ser6=
NM_001142459.1:c.18T=	NP_001135931.2:p.Ser6=
NM_001142460.1:c.18T=	NP_001135932.2:p.Ser6=
NM_080871.3:c.271+339T=	NP_543147.2:n.271+339T=
XM_005249949.3:c.153T=	XP_005250006.1:p.Ser51=
NM_001142459.2:c.18T= MANE Select	NP_001135931.2:p.Ser6=
NM_080871.4:c.271+339T=	NP_543147.2:n.271+339T=