Canonical Allele Identifier: CA499355309

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325777C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998759C>A , CM000679.2:g.30998759C>A	GRCh38
NC_000017.10:g.29325777C>A , CM000679.1:g.29325777C>A	GRCh37
NC_000017.9:g.26349903C>A	NCBI36
NG_011701.1:g.32822C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.867C>A MANE Select	ENSP00000328340.5:p.Pro289=
ENST00000324689.8:c.*71C>A	ENSP00000323693.4:n.*71C>A
ENST00000328381.9:c.867C>A	ENSP00000328340.5:p.Pro289=
ENST00000443677.6:c.*71C>A	ENSP00000411965.2:n.*71C>A
ENST00000535306.6:c.*71C>A	ENSP00000440470.2:n.*71C>A
NM_001184992.1:c.*71C>A	NP_001171921.1:n.*71C>A
NM_032322.3:c.867C>A	NP_115698.3:p.Pro289=
NM_197939.1:c.*71C>A	NP_922921.1:n.*71C>A
XM_005258043.3:c.324C>A	XP_005258100.1:p.Pro108=
XM_006722138.2:c.546C>A	XP_006722201.1:p.Pro182=
XM_017025223.1:c.324C>A	XP_016880712.1:p.Pro108=
XM_024451000.1:c.324C>A	XP_024306768.1:p.Pro108=
XM_024451001.1:c.324C>A	XP_024306769.1:p.Pro108=
XR_002958077.1:n.1135C>A
NM_032322.4:c.867C>A MANE Select	NP_115698.3:p.Pro289=
NM_001184992.2:c.*71C>A	NP_001171921.1:n.*71C>A
NM_197939.2:c.*71C>A	NP_922921.1:n.*71C>A