Canonical Allele Identifier: CA652284300

Gene: ASB10

Linked Data

• COSMIC: COSN506019

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187265T>C , CM000669.2:g.151187265T>C	GRCh38
NC_000007.13:g.150884352T>C , CM000669.1:g.150884352T>C	GRCh37
NC_000007.12:g.150515285T>C	NCBI36
NG_017016.1:g.5568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-135A>G	ENSP00000275838.1:n.-135A>G
ENST00000377867.7:c.271+187A>G	ENSP00000367098.3:n.271+187A>G
ENST00000415615.1:c.*110A>G	ENSP00000410871.1:n.*110A>G
NM_001142459.1:c.-135A>G	NP_001135931.2:n.-135A>G
NM_001142460.1:c.-135A>G	NP_001135932.2:n.-135A>G
NM_080871.3:c.271+187A>G	NP_543147.2:n.271+187A>G
XM_005249949.3:c.1A>G	XP_005250006.1:p.Met1Val
NM_080871.4:c.271+187A>G	NP_543147.2:n.271+187A>G