Canonical Allele Identifier: CA399203309

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325870G>T (hg19) ; chr17:g.30998852G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998852G>T , CM000679.2:g.30998852G>T	GRCh38
NC_000017.10:g.29325870G>T , CM000679.1:g.29325870G>T	GRCh37
NC_000017.9:g.26349996G>T	NCBI36
NG_011701.1:g.32915G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.960G>T MANE Select	ENSP00000328340.5:p.Arg320Ser
ENST00000324689.8:c.*164G>T	ENSP00000323693.4:n.*164G>T
ENST00000328381.9:c.960G>T	ENSP00000328340.5:p.Arg320Ser
ENST00000443677.6:c.*164G>T	ENSP00000411965.2:n.*164G>T
ENST00000535306.6:c.*164G>T	ENSP00000440470.2:n.*164G>T
NM_001184992.1:c.*164G>T	NP_001171921.1:n.*164G>T
NM_032322.3:c.960G>T	NP_115698.3:p.Arg320Ser
NM_197939.1:c.*164G>T	NP_922921.1:n.*164G>T
XM_005258043.3:c.417G>T	XP_005258100.1:p.Arg139Ser
XM_006722138.2:c.639G>T	XP_006722201.1:p.Arg213Ser
XM_017025223.1:c.417G>T	XP_016880712.1:p.Arg139Ser
XM_024451000.1:c.417G>T	XP_024306768.1:p.Arg139Ser
XM_024451001.1:c.417G>T	XP_024306769.1:p.Arg139Ser
XR_002958077.1:n.1228G>T
NM_032322.4:c.960G>T MANE Select	NP_115698.3:p.Arg320Ser
NM_001184992.2:c.*164G>T	NP_001171921.1:n.*164G>T
NM_197939.2:c.*164G>T	NP_922921.1:n.*164G>T