Canonical Allele Identifier: CA625785802

Gene: RNF135

Linked Data

• dbSNP Id: rs1249485605
• gnomAD v2: 17-29325674-C-T
• gnomAD v3: 17-30998656-C-T
• gnomAD v4: 17-30998656-C-T
• MyVariant Identifiers: chr17:g.29325674C>T (hg19) ; chr17:g.30998656C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998656C>T , CM000679.2:g.30998656C>T	GRCh38
NC_000017.10:g.29325674C>T , CM000679.1:g.29325674C>T	GRCh37
NC_000017.9:g.26349800C>T	NCBI36
NG_011701.1:g.32719C>T

Transcript Alleles

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