Canonical Allele Identifier: CA399203330

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325878G>C (hg19) ; chr17:g.30998860G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998860G>C , CM000679.2:g.30998860G>C	GRCh38
NC_000017.10:g.29325878G>C , CM000679.1:g.29325878G>C	GRCh37
NC_000017.9:g.26350004G>C	NCBI36
NG_011701.1:g.32923G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.968G>C MANE Select	ENSP00000328340.5:p.Ser323Thr
ENST00000324689.8:c.*172G>C	ENSP00000323693.4:n.*172G>C
ENST00000328381.9:c.968G>C	ENSP00000328340.5:p.Ser323Thr
ENST00000443677.6:c.*172G>C	ENSP00000411965.2:n.*172G>C
ENST00000535306.6:c.*172G>C	ENSP00000440470.2:n.*172G>C
NM_001184992.1:c.*172G>C	NP_001171921.1:n.*172G>C
NM_032322.3:c.968G>C	NP_115698.3:p.Ser323Thr
NM_197939.1:c.*172G>C	NP_922921.1:n.*172G>C
XM_005258043.3:c.425G>C	XP_005258100.1:p.Ser142Thr
XM_006722138.2:c.647G>C	XP_006722201.1:p.Ser216Thr
XM_017025223.1:c.425G>C	XP_016880712.1:p.Ser142Thr
XM_024451000.1:c.425G>C	XP_024306768.1:p.Ser142Thr
XM_024451001.1:c.425G>C	XP_024306769.1:p.Ser142Thr
XR_002958077.1:n.1236G>C
NM_032322.4:c.968G>C MANE Select	NP_115698.3:p.Ser323Thr
NM_001184992.2:c.*172G>C	NP_001171921.1:n.*172G>C
NM_197939.2:c.*172G>C	NP_922921.1:n.*172G>C