Canonical Allele Identifier: CA2809186931

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998665_30998666insTTTTTTTGTT , CM000679.2:g.30998665_30998666insTTTTTTTGTT	GRCh38
NC_000017.10:g.29325683_29325684insTTTTTTTGTT , CM000679.1:g.29325683_29325684insTTTTTTTGTT	GRCh37
NC_000017.9:g.26349809_26349810insTTTTTTTGTT	NCBI36
NG_011701.1:g.32728_32729insTTTTTTTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.773_774insTTTTTTTGTT MANE Select	ENSP00000328340.5:p.Ile259PhefsTer9
ENST00000324689.8:c.610_611insTTTTTTTGTT	ENSP00000323693.4:p.Pro204LeufsTer?
ENST00000328381.9:c.773_774insTTTTTTTGTT	ENSP00000328340.5:p.Ile259PhefsTer9
ENST00000443677.6:c.466_467insTTTTTTTGTT	ENSP00000411965.2:p.Pro156LeufsTer?
ENST00000535306.6:c.838_839insTTTTTTTGTT	ENSP00000440470.2:p.Pro280LeufsTer?
NM_001184992.1:c.838_839insTTTTTTTGTT	NP_001171921.1:p.Pro280LeufsTer?
NM_032322.3:c.773_774insTTTTTTTGTT	NP_115698.3:p.Ile259PhefsTer9
NM_197939.1:c.610_611insTTTTTTTGTT	NP_922921.1:p.Pro204LeufsTer?
XM_005258043.3:c.230_231insTTTTTTTGTT	XP_005258100.1:p.Ile78PhefsTer9
XM_006722138.2:c.452_453insTTTTTTTGTT	XP_006722201.1:p.Ile152PhefsTer9
XM_017025223.1:c.230_231insTTTTTTTGTT	XP_016880712.1:p.Ile78PhefsTer9
XM_024451000.1:c.230_231insTTTTTTTGTT	XP_024306768.1:p.Ile78PhefsTer9
XM_024451001.1:c.230_231insTTTTTTTGTT	XP_024306769.1:p.Ile78PhefsTer9
XR_002958076.1:n.1106_1107insTTTTTTTGTT
XR_002958077.1:n.1041_1042insTTTTTTTGTT
XR_002958078.1:n.878_879insTTTTTTTGTT
NM_032322.4:c.773_774insTTTTTTTGTT MANE Select	NP_115698.3:p.Ile259PhefsTer9
NM_001184992.2:c.838_839insTTTTTTTGTT	NP_001171921.1:p.Pro280LeufsTer?
NM_197939.2:c.610_611insTTTTTTTGTT	NP_922921.1:p.Pro204LeufsTer?