Canonical Allele Identifier: CA557902

Gene: RNF207

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6210215T>C , CM000663.2:g.6210215T>C	GRCh38
NC_000001.10:g.6270275T>C , CM000663.1:g.6270275T>C	GRCh37
NC_000001.9:g.6192862T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_207396.3:c.801-8T>C MANE Select	NP_997279.2:n.801-8T>C
ENST00000377939.5:c.801-8T>C MANE Select	ENSP00000367173.4:n.801-8T>C
NM_207396.2:c.801-8T>C	NP_997279.2:n.801-8T>C
ENST00000377939.4:c.801-8T>C	ENSP00000367173.4:n.801-8T>C
ENST00000485539.5:n.810-8T>C
ENST00000496676.5:n.340-8T>C
XM_011541438.1:c.801-8T>C	XP_011539740.1:n.801-8T>C
XM_011541439.1:c.945-8T>C	XP_011539741.1:n.945-8T>C
XM_011541439.3:c.945-8T>C	XP_011539741.1:n.945-8T>C
XM_011541440.1:c.945-8T>C	XP_011539742.1:n.945-8T>C
XM_017001259.2:c.801-8T>C	XP_016856748.1:n.801-8T>C
XR_001737158.2:n.967-8T>C
XR_001737159.2:n.967-8T>C
XR_001737161.2:n.967-8T>C
XR_001737162.2:n.967-8T>C
XR_001737164.2:n.953-8T>C
XR_002956484.1:n.967-8T>C
XR_002956486.1:n.967-8T>C
XR_946651.1:n.1110-8T>C
XR_946651.3:n.967-8T>C
XR_946652.1:n.1110-8T>C
XR_946652.3:n.967-8T>C