Canonical Allele Identifier: CA399203119

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325786G>C (hg19) ; chr17:g.30998768G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998768G>C , CM000679.2:g.30998768G>C	GRCh38
NC_000017.10:g.29325786G>C , CM000679.1:g.29325786G>C	GRCh37
NC_000017.9:g.26349912G>C	NCBI36
NG_011701.1:g.32831G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.876G>C MANE Select	ENSP00000328340.5:p.Trp292Cys
ENST00000324689.8:c.*80G>C	ENSP00000323693.4:n.*80G>C
ENST00000328381.9:c.876G>C	ENSP00000328340.5:p.Trp292Cys
ENST00000443677.6:c.*80G>C	ENSP00000411965.2:n.*80G>C
ENST00000535306.6:c.*80G>C	ENSP00000440470.2:n.*80G>C
NM_001184992.1:c.*80G>C	NP_001171921.1:n.*80G>C
NM_032322.3:c.876G>C	NP_115698.3:p.Trp292Cys
NM_197939.1:c.*80G>C	NP_922921.1:n.*80G>C
XM_005258043.3:c.333G>C	XP_005258100.1:p.Trp111Cys
XM_006722138.2:c.555G>C	XP_006722201.1:p.Trp185Cys
XM_017025223.1:c.333G>C	XP_016880712.1:p.Trp111Cys
XM_024451000.1:c.333G>C	XP_024306768.1:p.Trp111Cys
XM_024451001.1:c.333G>C	XP_024306769.1:p.Trp111Cys
XR_002958077.1:n.1144G>C
NM_032322.4:c.876G>C MANE Select	NP_115698.3:p.Trp292Cys
NM_001184992.2:c.*80G>C	NP_001171921.1:n.*80G>C
NM_197939.2:c.*80G>C	NP_922921.1:n.*80G>C