Canonical Allele Identifier: CA1433107989

Gene: RNF212

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1084399G>T , CM000666.2:g.1084399G>T	GRCh38
NC_000004.11:g.1078187G>T , CM000666.1:g.1078187G>T	GRCh37
NC_000004.10:g.1068187G>T	NCBI36
NG_027812.1:g.34166C>A
NG_027812.2:g.34396C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698262.1:c.362+1497C>A	ENSP00000513634.1:n.362+1497C>A
ENST00000433731.7:c.362+1497C>A MANE Select	ENSP00000389709.2:n.362+1497C>A
ENST00000382968.9:c.362+1497C>A	ENSP00000372428.5:n.362+1497C>A
ENST00000433731.6:c.362+1497C>A	ENSP00000389709.2:n.362+1497C>A
ENST00000506730.5:c.*141+1497C>A	ENSP00000425843.1:n.*141+1497C>A
ENST00000508428.5:c.*141+1497C>A	ENSP00000423030.1:n.*141+1497C>A
ENST00000510715.5:c.*226+1497C>A	ENSP00000423560.1:n.*226+1497C>A
ENST00000511620.5:c.362+1497C>A	ENSP00000426115.1:n.362+1497C>A
NM_001131034.3:c.362+1497C>A	NP_001124506.1:n.362+1497C>A
NM_194439.4:c.362+1497C>A	NP_919420.1:n.362+1497C>A
XM_005272274.2:c.362+1497C>A	XP_005272331.1:n.362+1497C>A
XM_011513438.1:c.230+1497C>A	XP_011511740.1:n.230+1497C>A
XM_011513439.1:c.230+1497C>A	XP_011511741.1:n.230+1497C>A
XM_011513440.1:c.362+1497C>A	XP_011511742.1:n.362+1497C>A
XM_011513441.1:c.362+1497C>A	XP_011511743.1:n.362+1497C>A
XM_011513442.1:c.164+1497C>A	XP_011511744.1:n.164+1497C>A
XM_011513443.1:c.164+1497C>A	XP_011511745.1:n.164+1497C>A
XM_011513444.1:c.362+1497C>A	XP_011511746.1:n.362+1497C>A
XM_011513445.1:c.247-10737C>A	XP_011511747.1:n.247-10737C>A
XM_011513446.1:c.247-10737C>A	XP_011511748.1:n.247-10737C>A
XR_246609.2:n.463+1497C>A
XR_924933.1:n.460+1497C>A
XR_924936.1:n.460+1497C>A
XR_924937.1:n.460+1497C>A
NM_001366918.1:c.362+1497C>A	NP_001353847.1:n.362+1497C>A
NM_001366919.1:c.362+1497C>A	NP_001353848.1:n.362+1497C>A
NR_159497.1:n.462+1497C>A
NR_159498.1:n.462+1497C>A
NR_159499.1:n.285-10737C>A
NR_159500.1:n.497-10737C>A
NR_159501.1:n.674+1497C>A
NR_159502.1:n.462+1497C>A
NR_159503.1:n.400+1497C>A
NR_159504.1:n.400+1497C>A
NR_159505.1:n.400+1497C>A
XM_011513445.2:c.247-10737C>A	XP_011511747.1:n.247-10737C>A
XM_017008039.1:c.230+1497C>A	XP_016863528.1:n.230+1497C>A
XM_017008040.1:c.230+1497C>A	XP_016863529.1:n.230+1497C>A
XR_001741208.1:n.460+1497C>A
XR_002959724.1:n.460+1497C>A
NM_001131034.4:c.362+1497C>A MANE Select	NP_001124506.1:n.362+1497C>A
NM_194439.5:c.362+1497C>A	NP_919420.1:n.362+1497C>A