Canonical Allele Identifier: CA2255462350

Gene: RNF135

Linked Data

• dbSNP Id: rs1908512619

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998403_30998406del , CM000679.2:g.30998403_30998406del	GRCh38
NC_000017.10:g.29325421_29325424del , CM000679.1:g.29325421_29325424del	GRCh37
NC_000017.9:g.26349547_26349550del	NCBI36
NG_011701.1:g.32466_32469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-259_770-256del MANE Select	ENSP00000328340.5:n.770-259_770-256del
ENST00000324689.8:c.607-259_607-256del	ENSP00000323693.4:n.607-259_607-256del
ENST00000328381.9:c.770-259_770-256del	ENSP00000328340.5:n.770-259_770-256del
ENST00000443677.6:c.463-259_463-256del	ENSP00000411965.2:n.463-259_463-256del
ENST00000535306.6:c.835-259_835-256del	ENSP00000440470.2:n.835-259_835-256del
NM_001184992.1:c.835-259_835-256del	NP_001171921.1:n.835-259_835-256del
NM_032322.3:c.770-259_770-256del	NP_115698.3:n.770-259_770-256del
NM_197939.1:c.607-259_607-256del	NP_922921.1:n.607-259_607-256del
XM_005258043.3:c.227-259_227-256del	XP_005258100.1:n.227-259_227-256del
XM_006722138.2:c.449-259_449-256del	XP_006722201.1:n.449-259_449-256del
XM_017025223.1:c.227-259_227-256del	XP_016880712.1:n.227-259_227-256del
XM_024451000.1:c.227-259_227-256del	XP_024306768.1:n.227-259_227-256del
XM_024451001.1:c.227-259_227-256del	XP_024306769.1:n.227-259_227-256del
XR_002958076.1:n.1103-259_1103-256del
XR_002958077.1:n.1038-259_1038-256del
XR_002958078.1:n.875-259_875-256del
NM_032322.4:c.770-259_770-256del MANE Select	NP_115698.3:n.770-259_770-256del
NM_001184992.2:c.835-259_835-256del	NP_001171921.1:n.835-259_835-256del
NM_197939.2:c.607-259_607-256del	NP_922921.1:n.607-259_607-256del