Canonical Allele Identifier: CA411094932

Gene: ZNRF3

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29042493A>G , CM000684.2:g.29042493A>G	GRCh38
NC_000022.10:g.29438481A>G , CM000684.1:g.29438481A>G	GRCh37
NC_000022.9:g.27768481A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544604.7:c.427-2A>G MANE Select	ENSP00000443824.2:n.427-2A>G
ENST00000402174.5:c.127-2A>G	ENSP00000384456.1:n.127-2A>G
ENST00000406323.3:c.127-2A>G	ENSP00000384553.3:n.127-2A>G
ENST00000544604.6:c.427-2A>G	ENSP00000443824.2:n.427-2A>G
NM_001206998.1:c.427-2A>G	NP_001193927.1:n.427-2A>G
NM_032173.3:c.127-2A>G	NP_115549.2:n.127-2A>G
XM_005261773.2:c.127-2A>G	XP_005261830.1:n.127-2A>G
XM_011530434.1:c.175-2A>G	XP_011528736.1:n.175-2A>G
XM_011530435.1:c.142-2A>G	XP_011528737.1:n.142-2A>G
XM_011530436.1:c.142-2A>G	XP_011528738.1:n.142-2A>G
XM_011530437.1:c.142-2A>G	XP_011528739.1:n.142-2A>G
XM_011530438.1:c.142-2A>G	XP_011528740.1:n.142-2A>G
XM_011530439.1:c.139-2A>G	XP_011528741.1:n.139-2A>G
XM_011530440.1:c.127-2A>G	XP_011528742.1:n.127-2A>G
XM_011530441.1:c.127-2A>G	XP_011528743.1:n.127-2A>G
XM_011530435.2:c.142-2A>G	XP_011528737.1:n.142-2A>G
XM_011530436.3:c.142-2A>G	XP_011528738.1:n.142-2A>G
XM_011530438.2:c.142-2A>G	XP_011528740.1:n.142-2A>G
XM_017028990.1:c.142-2A>G	XP_016884479.1:n.142-2A>G
XM_024452286.1:c.-147-2A>G	XP_024308054.1:n.-147-2A>G
NM_001206998.2:c.427-2A>G MANE Select	NP_001193927.1:n.427-2A>G
NM_032173.4:c.127-2A>G	NP_115549.2:n.127-2A>G