Canonical Allele Identifier: CA2739944778

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187249C>G , CM000669.2:g.151187249C>G	GRCh38
NC_000007.13:g.150884336C>G , CM000669.1:g.150884336C>G	GRCh37
NC_000007.12:g.150515269C>G	NCBI36
NG_017016.1:g.5584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-119G>C MANE Select	ENSP00000391137.2:n.-119G>C
ENST00000275838.5:c.-119G>C	ENSP00000275838.1:n.-119G>C
ENST00000377867.7:c.271+203G>C	ENSP00000367098.3:n.271+203G>C
ENST00000415615.1:c.*121+5G>C	ENSP00000410871.1:n.*121+5G>C
NM_001142459.1:c.-119G>C	NP_001135931.2:n.-119G>C
NM_001142460.1:c.-119G>C	NP_001135932.2:n.-119G>C
NM_080871.3:c.271+203G>C	NP_543147.2:n.271+203G>C
XM_005249949.3:c.17G>C	XP_005250006.1:p.Ser6Thr
NM_001142459.2:c.-119G>C MANE Select	NP_001135931.2:n.-119G>C
NM_080871.4:c.271+203G>C	NP_543147.2:n.271+203G>C