Canonical Allele Identifier: CA399203054

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325754A>G (hg19) ; chr17:g.30998736A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998736A>G , CM000679.2:g.30998736A>G	GRCh38
NC_000017.10:g.29325754A>G , CM000679.1:g.29325754A>G	GRCh37
NC_000017.9:g.26349880A>G	NCBI36
NG_011701.1:g.32799A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.844A>G MANE Select	ENSP00000328340.5:p.Thr282Ala
ENST00000324689.8:c.*48A>G	ENSP00000323693.4:n.*48A>G
ENST00000328381.9:c.844A>G	ENSP00000328340.5:p.Thr282Ala
ENST00000443677.6:c.*48A>G	ENSP00000411965.2:n.*48A>G
ENST00000535306.6:c.*48A>G	ENSP00000440470.2:n.*48A>G
NM_001184992.1:c.*48A>G	NP_001171921.1:n.*48A>G
NM_032322.3:c.844A>G	NP_115698.3:p.Thr282Ala
NM_197939.1:c.*48A>G	NP_922921.1:n.*48A>G
XM_005258043.3:c.301A>G	XP_005258100.1:p.Thr101Ala
XM_006722138.2:c.523A>G	XP_006722201.1:p.Thr175Ala
XM_017025223.1:c.301A>G	XP_016880712.1:p.Thr101Ala
XM_024451000.1:c.301A>G	XP_024306768.1:p.Thr101Ala
XM_024451001.1:c.301A>G	XP_024306769.1:p.Thr101Ala
XR_002958076.1:n.1177A>G
XR_002958077.1:n.1112A>G
XR_002958078.1:n.949A>G
NM_032322.4:c.844A>G MANE Select	NP_115698.3:p.Thr282Ala
NM_001184992.2:c.*48A>G	NP_001171921.1:n.*48A>G
NM_197939.2:c.*48A>G	NP_922921.1:n.*48A>G