Canonical Allele Identifier: CA2625000016
Gene: TMEM260 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.56621706_56621709del , CM000676.2:g.56621706_56621709del GRCh38
NC_000014.8:g.57088424_57088427del , CM000676.1:g.57088424_57088427del GRCh37
NC_000014.7:g.56158177_56158180del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261556.11:c.1398+4_1398+7del
ENST00000261556.10:c.1398+4_1398+7del
ENST00000538838.5:c.1226+2943_1226+2946del ENSP00000441934.1:n.1226+2943_1226+2946de...
ENST00000539559.6:c.*308+4_*308+7del
ENST00000555497.5:c.*700+2943_*700+2946del ENSP00000452065.1:n.*700+2943_*700+2946de...
ENST00000555905.5:c.440+2943_440+2946del
ENST00000556422.5:c.758+2943_758+2946del ENSP00000450988.1:n.758+2943_758+2946del
ENST00000556648.1:n.862+2943_862+2946del
NM_017799.3:c.1398+4_1398+7del
XM_005267771.1:c.357+4_357+7del
XM_006720176.1:c.558+4_558+7del
XM_006720178.1:c.357+4_357+7del
XM_011536850.1:c.1226+2943_1226+2946del XP_011535152.1:n.1226+2943_1226+2946del
XM_011536851.1:c.1398+4_1398+7del
XM_011536852.1:c.1047+4_1047+7del
XM_011536853.1:c.930+4_930+7del
XM_011536855.1:c.525+4_525+7del
XM_011536856.1:c.357+4_357+7del
XR_245695.1:n.1350+2943_1350+2946del
XR_943481.1:n.1522+4_1522+7del
XM_011536851.2:c.1398+4_1398+7del
XM_017021379.2:c.1398+4_1398+7del
XM_017021380.1:c.558+4_558+7del
XM_024449636.1:c.357+4_357+7del
XR_001750382.2:n.1521+4_1521+7del
XR_001750384.2:n.1592+4_1592+7del
XR_001750385.2:n.1615+4_1615+7del
XR_001750386.2:n.1686+4_1686+7del
XR_001750387.2:n.1349+2943_1349+2946del
XR_245695.2:n.1349+2943_1349+2946del
NM_017799.4:c.1398+4_1398+7del