Canonical Allele Identifier: CA399203100

Gene: RNF135

Linked Data

• dbSNP Id: rs1229296082
• gnomAD v2: 17-29325776-C-T
• gnomAD v3: 17-30998758-C-T
• gnomAD v4: 17-30998758-C-T
• MyVariant Identifiers: chr17:g.29325776C>T (hg19) ; chr17:g.30998758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998758C>T , CM000679.2:g.30998758C>T	GRCh38
NC_000017.10:g.29325776C>T , CM000679.1:g.29325776C>T	GRCh37
NC_000017.9:g.26349902C>T	NCBI36
NG_011701.1:g.32821C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000328381.10:c.866C>T MANE Select	ENSP00000328340.5:p.Pro289Leu
ENST00000324689.8:c.*70C>T	ENSP00000323693.4:n.*70C>T
ENST00000328381.9:c.866C>T	ENSP00000328340.5:p.Pro289Leu
ENST00000443677.6:c.*70C>T	ENSP00000411965.2:n.*70C>T
ENST00000535306.6:c.*70C>T	ENSP00000440470.2:n.*70C>T
NM_001184992.1:c.*70C>T	NP_001171921.1:n.*70C>T
NM_032322.3:c.866C>T	NP_115698.3:p.Pro289Leu
NM_197939.1:c.*70C>T	NP_922921.1:n.*70C>T
XM_005258043.3:c.323C>T	XP_005258100.1:p.Pro108Leu
XM_006722138.2:c.545C>T	XP_006722201.1:p.Pro182Leu
XM_017025223.1:c.323C>T	XP_016880712.1:p.Pro108Leu
XM_024451000.1:c.323C>T	XP_024306768.1:p.Pro108Leu
XM_024451001.1:c.323C>T	XP_024306769.1:p.Pro108Leu
XR_002958077.1:n.1134C>T
NM_032322.4:c.866C>T MANE Select	NP_115698.3:p.Pro289Leu
NM_001184992.2:c.*70C>T	NP_001171921.1:n.*70C>T
NM_197939.2:c.*70C>T	NP_922921.1:n.*70C>T