Canonical Allele Identifier: CA499355304

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325771A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998753A>C , CM000679.2:g.30998753A>C	GRCh38
NC_000017.10:g.29325771A>C , CM000679.1:g.29325771A>C	GRCh37
NC_000017.9:g.26349897A>C	NCBI36
NG_011701.1:g.32816A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328381.10:c.861A>C MANE Select	ENSP00000328340.5:p.Pro287=
ENST00000324689.8:c.*65A>C	ENSP00000323693.4:n.*65A>C
ENST00000328381.9:c.861A>C	ENSP00000328340.5:p.Pro287=
ENST00000443677.6:c.*65A>C	ENSP00000411965.2:n.*65A>C
ENST00000535306.6:c.*65A>C	ENSP00000440470.2:n.*65A>C
NM_001184992.1:c.*65A>C	NP_001171921.1:n.*65A>C
NM_032322.3:c.861A>C	NP_115698.3:p.Pro287=
NM_197939.1:c.*65A>C	NP_922921.1:n.*65A>C
XM_005258043.3:c.318A>C	XP_005258100.1:p.Pro106=
XM_006722138.2:c.540A>C	XP_006722201.1:p.Pro180=
XM_017025223.1:c.318A>C	XP_016880712.1:p.Pro106=
XM_024451000.1:c.318A>C	XP_024306768.1:p.Pro106=
XM_024451001.1:c.318A>C	XP_024306769.1:p.Pro106=
XR_002958077.1:n.1129A>C
NM_032322.4:c.861A>C MANE Select	NP_115698.3:p.Pro287=
NM_001184992.2:c.*65A>C	NP_001171921.1:n.*65A>C
NM_197939.2:c.*65A>C	NP_922921.1:n.*65A>C