Canonical Allele Identifier: CA399202897

Gene: RNF135

Linked Data

• dbSNP Id: rs772497150
• gnomAD v3: 17-30998667-A-C
• gnomAD v4: 17-30998667-A-C
• MyVariant Identifiers: chr17:g.29325685A>C (hg19) ; chr17:g.30998667A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998667A>C , CM000679.2:g.30998667A>C	GRCh38
NC_000017.10:g.29325685A>C , CM000679.1:g.29325685A>C	GRCh37
NC_000017.9:g.26349811A>C	NCBI36
NG_011701.1:g.32730A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.775A>C MANE Select	ENSP00000328340.5:p.Ile259Leu
ENST00000324689.8:c.612A>C	ENSP00000323693.4:p.Pro204=
ENST00000328381.9:c.775A>C	ENSP00000328340.5:p.Ile259Leu
ENST00000443677.6:c.468A>C	ENSP00000411965.2:p.Pro156=
ENST00000535306.6:c.840A>C	ENSP00000440470.2:p.Pro280=
NM_001184992.1:c.840A>C	NP_001171921.1:p.Pro280=
NM_032322.3:c.775A>C	NP_115698.3:p.Ile259Leu
NM_197939.1:c.612A>C	NP_922921.1:p.Pro204=
XM_005258043.3:c.232A>C	XP_005258100.1:p.Ile78Leu
XM_006722138.2:c.454A>C	XP_006722201.1:p.Ile152Leu
XM_017025223.1:c.232A>C	XP_016880712.1:p.Ile78Leu
XM_024451000.1:c.232A>C	XP_024306768.1:p.Ile78Leu
XM_024451001.1:c.232A>C	XP_024306769.1:p.Ile78Leu
XR_002958076.1:n.1108A>C
XR_002958077.1:n.1043A>C
XR_002958078.1:n.880A>C
NM_032322.4:c.775A>C MANE Select	NP_115698.3:p.Ile259Leu
NM_001184992.2:c.840A>C	NP_001171921.1:p.Pro280=
NM_197939.2:c.612A>C	NP_922921.1:p.Pro204=