Canonical Allele Identifier: CA392632669

Gene: SLTM RNF111

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58887316G>T , CM000677.2:g.58887316G>T	GRCh38
NC_000015.9:g.59179515G>T , CM000677.1:g.59179515G>T	GRCh37
NC_000015.8:g.56966807G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024755.4:c.2600C>A (SLTM) MANE Select	NP_079031.2:p.Pro867His
ENST00000380516.7:c.2600C>A (SLTM) MANE Select	ENSP00000369887.2:p.Pro867His
NM_001013843.1:c.2546C>A (SLTM)	NP_001013865.1:p.Pro849His
NM_001013843.2:c.2546C>A (SLTM)	NP_001013865.1:p.Pro849His
NM_001013843.3:c.2546C>A (SLTM)	NP_001013865.1:p.Pro849His
NM_024755.2:c.2600C>A (SLTM)	NP_079031.2:p.Pro867His
NM_024755.3:c.2600C>A (SLTM)	NP_079031.2:p.Pro867His
NR_135042.1:n.2044C>A (SLTM)
NR_135042.2:n.2047C>A (SLTM)
NR_135043.1:n.2154C>A (SLTM)
NR_135043.2:n.2157C>A (SLTM)
ENST00000380516.6:c.2600C>A (SLTM)	ENSP00000369887.2:p.Pro867His
ENST00000432750.5:c.1298C>A (SLTM)	ENSP00000411534.1:p.Pro433His
ENST00000492526.5:c.*1399C>A (SLTM)	ENSP00000453711.1:n.*1399C>A
ENST00000557924.5:c.*1854C>A (SLTM)	ENSP00000454000.1:n.*1854C>A
ENST00000558052.1:n.263C>A (SLTM)
ENST00000559757.1:c.-20+22014G>T (RNF111)	ENSP00000452919.1:n.-20+22014G>T
ENST00000560695.1:n.570C>A (SLTM)
XM_006720686.2:c.2354C>A (SLTM)	XP_006720749.2:p.Pro785His
XM_006720686.3:c.2759C>A (SLTM)	XP_006720749.3:p.Pro920His
XM_006720690.1:c.1307C>A (SLTM)	XP_006720753.1:p.Pro436His
XM_011522022.1:c.3026C>A (SLTM)	XP_011520324.1:p.Pro1009His
XM_011522023.1:c.2972C>A (SLTM)	XP_011520325.1:p.Pro991His
XM_011522024.1:c.2876C>A (SLTM)	XP_011520326.1:p.Pro959His
XM_011522025.1:c.2828C>A (SLTM)	XP_011520327.1:p.Pro943His
XM_011522026.1:c.2402C>A (SLTM)	XP_011520328.1:p.Pro801His
XM_011522027.1:c.2780C>A (SLTM)	XP_011520329.1:p.Pro927His
XM_011522028.1:c.2726C>A (SLTM)	XP_011520330.1:p.Pro909His
XM_011522029.1:c.2462C>A (SLTM)	XP_011520331.1:p.Pro821His
XM_011522029.2:c.2462C>A (SLTM)	XP_011520331.1:p.Pro821His
XM_011522031.1:c.1916C>A (SLTM)	XP_011520333.1:p.Pro639His
XM_011522031.2:c.1916C>A (SLTM)	XP_011520333.1:p.Pro639His
XM_011522032.1:c.1307C>A (SLTM)	XP_011520334.1:p.Pro436His
XM_017022576.1:c.2396C>A (SLTM)	XP_016878065.1:p.Pro799His
XM_017022578.1:c.2705C>A (SLTM)	XP_016878067.1:p.Pro902His
XM_017022579.1:c.2441C>A (SLTM)	XP_016878068.1:p.Pro814His
XM_017022580.2:c.1307C>A (SLTM)	XP_016878069.1:p.Pro436His
XM_024450054.1:c.1916C>A (SLTM)	XP_024305822.1:p.Pro639His
XM_024450055.1:c.1196C>A (SLTM)	XP_024305823.1:p.Pro399His
XR_001751390.1:n.3188C>A (SLTM)
XR_001751391.2:n.2530C>A (SLTM)
XR_001751392.1:n.2476C>A (SLTM)
XR_001751393.1:n.2921C>A (SLTM)