Canonical Allele Identifier: CA2637065474

Gene: RNF135

Linked Data

• gnomAD v4: 17-30998515-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998515T>G , CM000679.2:g.30998515T>G	GRCh38
NC_000017.10:g.29325533T>G , CM000679.1:g.29325533T>G	GRCh37
NC_000017.9:g.26349659T>G	NCBI36
NG_011701.1:g.32578T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-147T>G MANE Select	ENSP00000328340.5:n.770-147T>G
ENST00000324689.8:c.607-147T>G	ENSP00000323693.4:n.607-147T>G
ENST00000328381.9:c.770-147T>G	ENSP00000328340.5:n.770-147T>G
ENST00000443677.6:c.463-147T>G	ENSP00000411965.2:n.463-147T>G
ENST00000535306.6:c.835-147T>G	ENSP00000440470.2:n.835-147T>G
NM_001184992.1:c.835-147T>G	NP_001171921.1:n.835-147T>G
NM_032322.3:c.770-147T>G	NP_115698.3:n.770-147T>G
NM_197939.1:c.607-147T>G	NP_922921.1:n.607-147T>G
XM_005258043.3:c.227-147T>G	XP_005258100.1:n.227-147T>G
XM_006722138.2:c.449-147T>G	XP_006722201.1:n.449-147T>G
XM_017025223.1:c.227-147T>G	XP_016880712.1:n.227-147T>G
XM_024451000.1:c.227-147T>G	XP_024306768.1:n.227-147T>G
XM_024451001.1:c.227-147T>G	XP_024306769.1:n.227-147T>G
XR_002958076.1:n.1103-147T>G
XR_002958077.1:n.1038-147T>G
XR_002958078.1:n.875-147T>G
NM_032322.4:c.770-147T>G MANE Select	NP_115698.3:n.770-147T>G
NM_001184992.2:c.835-147T>G	NP_001171921.1:n.835-147T>G
NM_197939.2:c.607-147T>G	NP_922921.1:n.607-147T>G