Canonical Allele Identifier: CA399202884

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325680G>T (hg19) ; chr17:g.30998662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998662G>T , CM000679.2:g.30998662G>T	GRCh38
NC_000017.10:g.29325680G>T , CM000679.1:g.29325680G>T	GRCh37
NC_000017.9:g.26349806G>T	NCBI36
NG_011701.1:g.32725G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770G>T MANE Select	ENSP00000328340.5:p.Trp257Leu
ENST00000324689.8:c.607G>T	ENSP00000323693.4:p.Gly203Trp
ENST00000328381.9:c.770G>T	ENSP00000328340.5:p.Trp257Leu
ENST00000443677.6:c.463G>T	ENSP00000411965.2:p.Gly155Trp
ENST00000535306.6:c.835G>T	ENSP00000440470.2:p.Gly279Trp
NM_001184992.1:c.835G>T	NP_001171921.1:p.Gly279Trp
NM_032322.3:c.770G>T	NP_115698.3:p.Trp257Leu
NM_197939.1:c.607G>T	NP_922921.1:p.Gly203Trp
XM_005258043.3:c.227G>T	XP_005258100.1:p.Trp76Leu
XM_006722138.2:c.449G>T	XP_006722201.1:p.Trp150Leu
XM_017025223.1:c.227G>T	XP_016880712.1:p.Trp76Leu
XM_024451000.1:c.227G>T	XP_024306768.1:p.Trp76Leu
XM_024451001.1:c.227G>T	XP_024306769.1:p.Trp76Leu
XR_002958076.1:n.1103G>T
XR_002958077.1:n.1038G>T
XR_002958078.1:n.875G>T
NM_032322.4:c.770G>T MANE Select	NP_115698.3:p.Trp257Leu
NM_001184992.2:c.835G>T	NP_001171921.1:p.Gly279Trp
NM_197939.2:c.607G>T	NP_922921.1:p.Gly203Trp