Canonical Allele Identifier: CA1752545969

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187143A= , CM000669.2:g.151187143A=	GRCh38
NC_000007.13:g.150884230A= , CM000669.1:g.150884230A=	GRCh37
NC_000007.12:g.150515163A=	NCBI36
NG_017016.1:g.5690T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-13T= MANE Select	ENSP00000391137.2:n.-13T=
ENST00000275838.5:c.-13T=	ENSP00000275838.1:n.-13T=
ENST00000377867.7:c.271+309T=	ENSP00000367098.3:n.271+309T=
ENST00000415615.1:c.*122-90T=	ENSP00000410871.1:n.*122-90T=
ENST00000420175.2:c.-13T=	ENSP00000391137.2:n.-13T=
NM_001142459.1:c.-13T=	NP_001135931.2:n.-13T=
NM_001142460.1:c.-13T=	NP_001135932.2:n.-13T=
NM_080871.3:c.271+309T=	NP_543147.2:n.271+309T=
XM_005249949.3:c.123T=	XP_005250006.1:p.Pro41=
NM_001142459.2:c.-13T= MANE Select	NP_001135931.2:n.-13T=
NM_080871.4:c.271+309T=	NP_543147.2:n.271+309T=