Canonical Allele Identifier: CA1752546021

Gene: ASB10

Linked Data

• dbSNP Id: rs1700234346

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187178G>A , CM000669.2:g.151187178G>A	GRCh38
NC_000007.13:g.150884265G>A , CM000669.1:g.150884265G>A	GRCh37
NC_000007.12:g.150515198G>A	NCBI36
NG_017016.1:g.5655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-48C>T MANE Select	ENSP00000391137.2:n.-48C>T
ENST00000275838.5:c.-48C>T	ENSP00000275838.1:n.-48C>T
ENST00000377867.7:c.271+274C>T	ENSP00000367098.3:n.271+274C>T
ENST00000415615.1:c.*121+76C>T	ENSP00000410871.1:n.*121+76C>T
NM_001142459.1:c.-48C>T	NP_001135931.2:n.-48C>T
NM_001142460.1:c.-48C>T	NP_001135932.2:n.-48C>T
NM_080871.3:c.271+274C>T	NP_543147.2:n.271+274C>T
XM_005249949.3:c.88C>T	XP_005250006.1:p.Pro30Ser
NM_001142459.2:c.-48C>T MANE Select	NP_001135931.2:n.-48C>T
NM_080871.4:c.271+274C>T	NP_543147.2:n.271+274C>T