Canonical Allele Identifier: CA2625000020

Gene: TMEM260

Linked Data

• gnomAD v4: 14-56621712-TGAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56621713_56621717del , CM000676.2:g.56621713_56621717del	GRCh38
NC_000014.8:g.57088431_57088435del , CM000676.1:g.57088431_57088435del	GRCh37
NC_000014.7:g.56158184_56158188del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1398+11_1398+15del MANE Select	ENSP00000261556.6:n.1398+11_1398+15del
ENST00000261556.10:c.1398+11_1398+15del	ENSP00000261556.6:n.1398+11_1398+15del
ENST00000538838.5:c.1226+2950_1226+2954del	ENSP00000441934.1:n.1226+2950_1226+2954de...
ENST00000539559.6:c.*308+11_*308+15del	ENSP00000442602.2:n.*308+11_*308+15del
ENST00000555497.5:c.*700+2950_*700+2954del	ENSP00000452065.1:n.*700+2950_*700+2954de...
ENST00000555905.5:c.440+2950_440+2954del
ENST00000556422.5:c.758+2950_758+2954del	ENSP00000450988.1:n.758+2950_758+2954del
ENST00000556648.1:n.862+2950_862+2954del
NM_017799.3:c.1398+11_1398+15del	NP_060269.3:n.1398+11_1398+15del
XM_005267771.1:c.357+11_357+15del	XP_005267828.1:n.357+11_357+15del
XM_006720176.1:c.558+11_558+15del	XP_006720239.1:n.558+11_558+15del
XM_006720178.1:c.357+11_357+15del	XP_006720241.1:n.357+11_357+15del
XM_011536850.1:c.1227-2949_1227-2945del	XP_011535152.1:n.1227-2949_1227-2945del
XM_011536851.1:c.1398+11_1398+15del	XP_011535153.1:n.1398+11_1398+15del
XM_011536852.1:c.1047+11_1047+15del	XP_011535154.1:n.1047+11_1047+15del
XM_011536853.1:c.930+11_930+15del	XP_011535155.1:n.930+11_930+15del
XM_011536855.1:c.525+11_525+15del	XP_011535157.1:n.525+11_525+15del
XM_011536856.1:c.357+11_357+15del	XP_011535158.1:n.357+11_357+15del
XR_245695.1:n.1350+2950_1350+2954del
XR_943481.1:n.1522+11_1522+15del
XM_011536851.2:c.1398+11_1398+15del	XP_011535153.1:n.1398+11_1398+15del
XM_017021379.2:c.1398+11_1398+15del	XP_016876868.1:n.1398+11_1398+15del
XM_017021380.1:c.558+11_558+15del	XP_016876869.1:n.558+11_558+15del
XM_024449636.1:c.357+11_357+15del	XP_024305404.1:n.357+11_357+15del
XR_001750382.2:n.1521+11_1521+15del
XR_001750384.2:n.1592+11_1592+15del
XR_001750385.2:n.1615+11_1615+15del
XR_001750386.2:n.1686+11_1686+15del
XR_001750387.2:n.1349+2950_1349+2954del
XR_245695.2:n.1349+2950_1349+2954del
NM_017799.4:c.1398+11_1398+15del MANE Select	NP_060269.3:n.1398+11_1398+15del