Canonical Allele Identifier: CA2739944619

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187133G>C , CM000669.2:g.151187133G>C	GRCh38
NC_000007.13:g.150884220G>C , CM000669.1:g.150884220G>C	GRCh37
NC_000007.12:g.150515153G>C	NCBI36
NG_017016.1:g.5700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-3C>G MANE Select	ENSP00000391137.2:n.-3C>G
ENST00000275838.5:c.-3C>G	ENSP00000275838.1:n.-3C>G
ENST00000377867.7:c.271+319C>G	ENSP00000367098.3:n.271+319C>G
ENST00000415615.1:c.*122-80C>G	ENSP00000410871.1:n.*122-80C>G
ENST00000420175.2:c.-3C>G	ENSP00000391137.2:n.-3C>G
NM_001142459.1:c.-3C>G	NP_001135931.2:n.-3C>G
NM_001142460.1:c.-3C>G	NP_001135932.2:n.-3C>G
NM_080871.3:c.271+319C>G	NP_543147.2:n.271+319C>G
XM_005249949.3:c.133C>G	XP_005250006.1:p.His45Asp
NM_001142459.2:c.-3C>G MANE Select	NP_001135931.2:n.-3C>G
NM_080871.4:c.271+319C>G	NP_543147.2:n.271+319C>G