Canonical Allele Identifier: CA3047142081

Gene: ZNRF3

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29048491_29048492delinsTT , CM000684.2:g.29048491_29048492delinsTT	GRCh38
NC_000022.10:g.29444479_29444480delinsTT , CM000684.1:g.29444479_29444480delinsTT	GRCh37
NC_000022.9:g.27774479_27774480delinsTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544604.7:c.1015_1015+1delinsTT
ENST00000402174.5:c.715_715+1delinsTT
ENST00000406323.3:c.715_715+1delinsTT
ENST00000544604.6:c.1015_1015+1delinsTT
NM_001206998.1:c.1015_1015+1delinsTT
NM_032173.3:c.715_715+1delinsTT
XM_005261773.2:c.715_715+1delinsTT
XM_011530434.1:c.763_763+1delinsTT
XM_011530435.1:c.730_730+1delinsTT
XM_011530436.1:c.730_730+1delinsTT
XM_011530437.1:c.730_730+1delinsTT
XM_011530438.1:c.730_730+1delinsTT
XM_011530439.1:c.727_727+1delinsTT
XM_011530440.1:c.715_715+1delinsTT
XM_011530441.1:c.715_715+1delinsTT
XM_011530435.2:c.730_730+1delinsTT
XM_011530436.3:c.730_730+1delinsTT
XM_011530438.2:c.730_730+1delinsTT
XM_017028990.1:c.730_730+1delinsTT
XM_024452286.1:c.442_442+1delinsTT
NM_001206998.2:c.1015_1015+1delinsTT
NM_032173.4:c.715_715+1delinsTT