Canonical Allele Identifier: CA14974636

Gene: ZNRF3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29054868C>T , CM000684.2:g.29054868C>T	GRCh38
NC_000022.10:g.29450856C>T , CM000684.1:g.29450856C>T	GRCh37
NC_000022.9:g.27780856C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544604.7:c.*1246C>T MANE Select	ENSP00000443824.2:n.*1246C>T
ENST00000544604.6:c.*1246C>T	ENSP00000443824.2:n.*1246C>T
NM_001206998.1:c.4057C>T	NP_001193927.1:n.4057C>T
NM_032173.3:c.*1246C>T	NP_115549.2:n.*1246C>T
XM_005261773.2:c.*1246C>T	XP_005261830.1:n.*1246C>T
XM_011530434.1:c.*1246C>T	XP_011528736.1:n.*1246C>T
XM_011530435.1:c.*1246C>T	XP_011528737.1:n.*1246C>T
XM_011530436.1:c.*1246C>T	XP_011528738.1:n.*1246C>T
XM_011530437.1:c.*1246C>T	XP_011528739.1:n.*1246C>T
XM_011530438.1:c.*1246C>T	XP_011528740.1:n.*1246C>T
XM_011530439.1:c.*1246C>T	XP_011528741.1:n.*1246C>T
XM_011530440.1:c.*1246C>T	XP_011528742.1:n.*1246C>T
XM_011530441.1:c.*1246C>T	XP_011528743.1:n.*1246C>T
XM_011530435.2:c.*1246C>T	XP_011528737.1:n.*1246C>T
XM_011530436.3:c.*1246C>T	XP_011528738.1:n.*1246C>T
XM_011530438.2:c.*1246C>T	XP_011528740.1:n.*1246C>T
XM_017028990.1:c.*1246C>T	XP_016884479.1:n.*1246C>T
XM_024452286.1:c.*1246C>T	XP_024308054.1:n.*1246C>T
NM_001206998.2:c.*1246C>T MANE Select	NP_001193927.1:n.*1246C>T
NM_032173.4:c.*1246C>T	NP_115549.2:n.*1246C>T