Canonical Allele Identifier: CA2079960635

Gene: RNF6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.26215127C= , CM000675.2:g.26215127C=	GRCh38
NC_000013.10:g.26789264C= , CM000675.1:g.26789264C=	GRCh37
NC_000013.9:g.25687264C=	NCBI36
NG_017042.1:g.12245G=
NG_017042.2:g.12245G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381588.9:c.755G= MANE Select	ENSP00000371000.4:p.Arg252=
ENST00000346166.7:c.755G=	ENSP00000342121.3:p.Arg252=
ENST00000381570.7:c.755G=	ENSP00000370982.3:p.Arg252=
ENST00000381588.8:c.755G=	ENSP00000371000.4:p.Arg252=
ENST00000468480.5:n.768+347G=
NM_005977.3:c.755G=	NP_005968.1:p.Arg252=
NM_183043.2:c.755G=	NP_898864.1:p.Arg252=
NM_183044.2:c.755G=	NP_898865.1:p.Arg252=
NM_183045.1:c.408+347G=	NP_898866.1:n.408+347G=
XM_005266485.1:c.755G=	XP_005266542.1:p.Arg252=
XM_005266486.1:c.755G=	XP_005266543.1:p.Arg252=
XM_011535177.1:c.755G=	XP_011533479.1:p.Arg252=
XM_011535178.1:c.408+347G=	XP_011533480.1:n.408+347G=
XM_005266485.3:c.755G=	XP_005266542.1:p.Arg252=
XM_005266486.2:c.755G=	XP_005266543.1:p.Arg252=
XM_011535177.3:c.755G=	XP_011533479.1:p.Arg252=
XM_011535178.2:c.408+347G=	XP_011533480.1:n.408+347G=
XM_017020685.2:c.408+347G=	XP_016876174.1:n.408+347G=
XM_017020686.1:c.408+347G=	XP_016876175.1:n.408+347G=
XM_017020687.1:c.408+347G=	XP_016876176.1:n.408+347G=
XM_024449390.1:c.755G=	XP_024305158.1:p.Arg252=
XM_024449391.1:c.408+347G=	XP_024305159.1:n.408+347G=
XM_024449392.1:c.408+347G=	XP_024305160.1:n.408+347G=
NM_005977.4:c.755G= MANE Select	NP_005968.1:p.Arg252=
NM_183043.3:c.755G=	NP_898864.1:p.Arg252=
NM_183044.3:c.755G=	NP_898865.1:p.Arg252=