Canonical Allele Identifier: CA129819682
Gene: RNF145 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1473247

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176563T>C , CM000667.2:g.159176563T>C GRCh38
NC_000005.9:g.158603571T>C , CM000667.1:g.158603571T>C GRCh37
NC_000005.8:g.158536149T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001199380.1:c.711+69A>G VV NP_001186309.1:p.=
NM_001199381.1:c.672+69A>G VV NP_001186310.1:p.=
NM_001199382.1:c.663+69A>G VV NP_001186311.1:p.=
NM_001199383.1:c.621+69A>G VV NP_001186312.1:p.=
NM_144726.2:c.705+69A>G VV NP_653327.1:p.=
XM_005265826.3:c.669+69A>G XP_005265883.1:p.=
XM_017009138.2:c.621+69A>G XP_016864627.1:p.=
XM_024454383.1:c.669+69A>G XP_024310151.1:p.=
ENST00000274542.6:c.705+69A>G ENSP00000274542.2:p.=
ENST00000424310.6:c.621+69A>G ENSP00000409064.2:p.=
ENST00000518802.5:c.711+69A>G ENSP00000430955.1:p.=
ENST00000519865.5:c.621+69A>G ENSP00000430397.1:p.=
ENST00000520638.1:c.663+69A>G ENSP00000429071.1:p.=
ENST00000521606.6:c.672+69A>G ENSP00000430753.2:p.=
ENST00000611185.4:c.621+69A>G ENSP00000482720.1:p.=