Canonical Allele Identifier: CA1139834723

Gene: RNF207

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6219310G= , CM000663.2:g.6219310G=	GRCh38
NC_000001.10:g.6279370G= , CM000663.1:g.6279370G=	GRCh37
NC_000001.9:g.6201957G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_207396.3:c.1808G= MANE Select	NP_997279.2:p.Gly603=
ENST00000377939.5:c.1808G= MANE Select	ENSP00000367173.4:p.Gly603=
NM_207396.2:c.1808G=	NP_997279.2:p.Gly603=
ENST00000377939.4:c.1808G=	ENSP00000367173.4:p.Gly603=
ENST00000483336.1:n.440G=
ENST00000496676.5:n.1525G=
XM_011541439.1:c.1952G=	XP_011539741.1:p.Gly651=
XM_011541439.3:c.1952G=	XP_011539741.1:p.Gly651=
XM_017001259.2:c.1874G=	XP_016856748.1:p.Gly625=
XR_001737158.2:n.2386G=
XR_001737159.2:n.2224G=
XR_001737162.2:n.2320G=
XR_001737164.2:n.2862G=
XR_946651.1:n.2301G=
XR_946651.3:n.2158G=
XR_946652.1:n.2287G=
XR_946652.3:n.2144G=