Canonical Allele Identifier: CA11743033

Gene: RNF212

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1058700A>G , CM000666.2:g.1058700A>G	GRCh38
NC_000004.11:g.1052488A>G , CM000666.1:g.1052488A>G	GRCh37
NC_000004.10:g.1042488A>G	NCBI36
NG_027812.2:g.60095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698262.1:c.575-307T>C	ENSP00000513634.1:n.575-307T>C
ENST00000503206.5:n.148-307T>C
ENST00000505693.5:n.502-307T>C
ENST00000506730.5:c.*354-307T>C	ENSP00000425843.1:n.*354-307T>C
ENST00000508633.5:n.157-307T>C
ENST00000514757.5:n.502-307T>C
XM_005272274.2:c.575-307T>C	XP_005272331.1:n.575-307T>C
XM_011513440.1:c.*23-307T>C	XP_011511742.1:n.*23-307T>C
XM_011513444.1:c.575-307T>C	XP_011511746.1:n.575-307T>C
XM_011513446.1:c.311-307T>C	XP_011511748.1:n.311-307T>C
XR_924933.1:n.873-307T>C
XR_924937.1:n.627-307T>C
NM_001366918.1:c.575-307T>C	NP_001353847.1:n.575-307T>C
NM_001366919.1:c.575-307T>C	NP_001353848.1:n.575-307T>C
XR_001741208.1:n.820-307T>C
XR_002959724.1:n.820-307T>C