Canonical Allele Identifier: CA1594978141

Gene: RNF145

Linked Data

• dbSNP Id: rs1784768675

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159177905_159177908dup , CM000667.2:g.159177905_159177908dup	GRCh38
NC_000005.9:g.158604913_158604916dup , CM000667.1:g.158604913_158604916dup	GRCh37
NC_000005.8:g.158537491_158537494dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000424310.7:c.386-1040_386-1037dup MANE Select	ENSP00000409064.2:n.386-1040_386-1037dup
ENST00000274542.6:c.470-1040_470-1037dup	ENSP00000274542.2:n.470-1040_470-1037dup
ENST00000424310.6:c.386-1040_386-1037dup	ENSP00000409064.2:n.386-1040_386-1037dup
ENST00000518802.5:c.476-1040_476-1037dup	ENSP00000430955.1:n.476-1040_476-1037dup
ENST00000519865.5:c.386-1040_386-1037dup	ENSP00000430397.1:n.386-1040_386-1037dup
ENST00000520638.1:c.428-1040_428-1037dup	ENSP00000429071.1:n.428-1040_428-1037dup
ENST00000521606.6:c.437-1040_437-1037dup	ENSP00000430753.2:n.437-1040_437-1037dup
ENST00000611185.4:c.386-1040_386-1037dup	ENSP00000482720.1:n.386-1040_386-1037dup
NM_001199380.1:c.476-1040_476-1037dup	NP_001186309.1:n.476-1040_476-1037dup
NM_001199381.1:c.437-1040_437-1037dup	NP_001186310.1:n.437-1040_437-1037dup
NM_001199382.1:c.428-1040_428-1037dup	NP_001186311.1:n.428-1040_428-1037dup
NM_001199383.1:c.386-1040_386-1037dup	NP_001186312.1:n.386-1040_386-1037dup
NM_144726.2:c.470-1040_470-1037dup	NP_653327.1:n.470-1040_470-1037dup
XM_005265826.3:c.434-1040_434-1037dup	XP_005265883.1:n.434-1040_434-1037dup
XM_017009138.2:c.386-1040_386-1037dup	XP_016864627.1:n.386-1040_386-1037dup
XM_024454383.1:c.434-1040_434-1037dup	XP_024310151.1:n.434-1040_434-1037dup
NM_001199381.2:c.437-1040_437-1037dup	NP_001186310.1:n.437-1040_437-1037dup
NM_001199383.2:c.386-1040_386-1037dup MANE Select	NP_001186312.1:n.386-1040_386-1037dup
NM_001199380.2:c.476-1040_476-1037dup	NP_001186309.1:n.476-1040_476-1037dup
NM_001199382.2:c.428-1040_428-1037dup	NP_001186311.1:n.428-1040_428-1037dup
NM_144726.3:c.470-1040_470-1037dup	NP_653327.1:n.470-1040_470-1037dup