Canonical Allele Identifier: CA2740699353

Gene: RNF145

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176495G>C , CM000667.2:g.159176495G>C	GRCh38
NC_000005.9:g.158603503G>C , CM000667.1:g.158603503G>C	GRCh37
NC_000005.8:g.158536081G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000424310.7:c.621+137C>G MANE Select	ENSP00000409064.2:n.621+137C>G
ENST00000274542.6:c.705+137C>G	ENSP00000274542.2:n.705+137C>G
ENST00000424310.6:c.621+137C>G	ENSP00000409064.2:n.621+137C>G
ENST00000518802.5:c.711+137C>G	ENSP00000430955.1:n.711+137C>G
ENST00000519865.5:c.621+137C>G	ENSP00000430397.1:n.621+137C>G
ENST00000520638.1:c.663+137C>G	ENSP00000429071.1:n.663+137C>G
ENST00000521606.6:c.672+137C>G	ENSP00000430753.2:n.672+137C>G
ENST00000611185.4:c.621+137C>G	ENSP00000482720.1:n.621+137C>G
NM_001199380.1:c.711+137C>G	NP_001186309.1:n.711+137C>G
NM_001199381.1:c.672+137C>G	NP_001186310.1:n.672+137C>G
NM_001199382.1:c.663+137C>G	NP_001186311.1:n.663+137C>G
NM_001199383.1:c.621+137C>G	NP_001186312.1:n.621+137C>G
NM_144726.2:c.705+137C>G	NP_653327.1:n.705+137C>G
XM_005265826.3:c.669+137C>G	XP_005265883.1:n.669+137C>G
XM_017009138.2:c.621+137C>G	XP_016864627.1:n.621+137C>G
XM_024454383.1:c.669+137C>G	XP_024310151.1:n.669+137C>G
NM_001199381.2:c.672+137C>G	NP_001186310.1:n.672+137C>G
NM_001199383.2:c.621+137C>G MANE Select	NP_001186312.1:n.621+137C>G
NM_001199380.2:c.711+137C>G	NP_001186309.1:n.711+137C>G
NM_001199382.2:c.663+137C>G	NP_001186311.1:n.663+137C>G
NM_144726.3:c.705+137C>G	NP_653327.1:n.705+137C>G