Canonical Allele Identifier: CA15837379

Gene: SLTM RNF111

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58882340G>T , CM000677.2:g.58882340G>T	GRCh38
NC_000015.9:g.59174539G>T , CM000677.1:g.59174539G>T	GRCh37
NC_000015.8:g.56961831G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380516.7:c.2996+1286C>A (SLTM) MANE Select	ENSP00000369887.2:n.2996+1286C>A
ENST00000380516.6:c.2996+1286C>A (SLTM)	ENSP00000369887.2:n.2996+1286C>A
ENST00000432750.5:c.1694+1286C>A (SLTM)	ENSP00000411534.1:n.1694+1286C>A
ENST00000492526.5:c.*1795+1286C>A (SLTM)	ENSP00000453711.1:n.*1795+1286C>A
ENST00000493062.5:n.311+1286C>A (SLTM)
ENST00000557924.5:c.*2250+1286C>A (SLTM)	ENSP00000454000.1:n.*2250+1286C>A
ENST00000559757.1:c.-20+17038G>T (RNF111)	ENSP00000452919.1:n.-20+17038G>T
ENST00000560494.1:c.194+1286C>A (SLTM)	ENSP00000452805.1:n.194+1286C>A
NM_001013843.1:c.2942+1286C>A (SLTM)	NP_001013865.1:n.2942+1286C>A
NM_024755.2:c.2996+1286C>A (SLTM)	NP_079031.2:n.2996+1286C>A
XM_006720686.2:c.2750+1286C>A (SLTM)	XP_006720749.2:n.2750+1286C>A
XM_006720690.1:c.1703+1286C>A (SLTM)	XP_006720753.1:n.1703+1286C>A
XM_011522022.1:c.3422+1286C>A (SLTM)	XP_011520324.1:n.3422+1286C>A
XM_011522023.1:c.3368+1286C>A (SLTM)	XP_011520325.1:n.3368+1286C>A
XM_011522024.1:c.3272+1286C>A (SLTM)	XP_011520326.1:n.3272+1286C>A
XM_011522025.1:c.3224+1286C>A (SLTM)	XP_011520327.1:n.3224+1286C>A
XM_011522026.1:c.2798+1286C>A (SLTM)	XP_011520328.1:n.2798+1286C>A
XM_011522027.1:c.3176+1286C>A (SLTM)	XP_011520329.1:n.3176+1286C>A
XM_011522028.1:c.3122+1286C>A (SLTM)	XP_011520330.1:n.3122+1286C>A
XM_011522029.1:c.2858+1286C>A (SLTM)	XP_011520331.1:n.2858+1286C>A
XM_011522031.1:c.2312+1286C>A (SLTM)	XP_011520333.1:n.2312+1286C>A
XM_011522032.1:c.1703+1286C>A (SLTM)	XP_011520334.1:n.1703+1286C>A
NM_001013843.2:c.2942+1286C>A (SLTM)	NP_001013865.1:n.2942+1286C>A
NM_024755.3:c.2996+1286C>A (SLTM)	NP_079031.2:n.2996+1286C>A
NR_135042.1:n.2440+1286C>A (SLTM)
NR_135043.1:n.2550+1286C>A (SLTM)
XM_006720686.3:c.3155+1286C>A (SLTM)	XP_006720749.3:n.3155+1286C>A
XM_011522029.2:c.2858+1286C>A (SLTM)	XP_011520331.1:n.2858+1286C>A
XM_011522031.2:c.2312+1286C>A (SLTM)	XP_011520333.1:n.2312+1286C>A
XM_017022576.1:c.2792+1286C>A (SLTM)	XP_016878065.1:n.2792+1286C>A
XM_017022578.1:c.3101+1286C>A (SLTM)	XP_016878067.1:n.3101+1286C>A
XM_017022579.1:c.2837+1286C>A (SLTM)	XP_016878068.1:n.2837+1286C>A
XM_017022580.2:c.1703+1286C>A (SLTM)	XP_016878069.1:n.1703+1286C>A
XM_024450054.1:c.2312+1286C>A (SLTM)	XP_024305822.1:n.2312+1286C>A
XM_024450055.1:c.1592+1286C>A (SLTM)	XP_024305823.1:n.1592+1286C>A
XR_001751390.1:n.3584+1286C>A (SLTM)
XR_001751391.2:n.2926+1286C>A (SLTM)
XR_001751392.1:n.2872+1286C>A (SLTM)
XR_001751393.1:n.3317+1286C>A (SLTM)
NM_024755.4:c.2996+1286C>A (SLTM) MANE Select	NP_079031.2:n.2996+1286C>A
NM_001013843.3:c.2942+1286C>A (SLTM)	NP_001013865.1:n.2942+1286C>A
NR_135042.2:n.2443+1286C>A (SLTM)
NR_135043.2:n.2553+1286C>A (SLTM)