Canonical Allele Identifier: CA2139044736

Gene: TMEM260

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56621710T= , CM000676.2:g.56621710T=	GRCh38
NC_000014.8:g.57088428T= , CM000676.1:g.57088428T=	GRCh37
NC_000014.7:g.56158181T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1398+8T= MANE Select	ENSP00000261556.6:n.1398+8T=
ENST00000261556.10:c.1398+8T=	ENSP00000261556.6:n.1398+8T=
ENST00000538838.5:c.1226+2947T=	ENSP00000441934.1:n.1226+2947T=
ENST00000539559.6:c.*308+8T=	ENSP00000442602.2:n.*308+8T=
ENST00000555497.5:c.*700+2947T=	ENSP00000452065.1:n.*700+2947T=
ENST00000555905.5:c.440+2947T=
ENST00000556422.5:c.758+2947T=	ENSP00000450988.1:n.758+2947T=
ENST00000556648.1:n.862+2947T=
NM_017799.3:c.1398+8T=	NP_060269.3:n.1398+8T=
XM_005267771.1:c.357+8T=	XP_005267828.1:n.357+8T=
XM_006720176.1:c.558+8T=	XP_006720239.1:n.558+8T=
XM_006720178.1:c.357+8T=	XP_006720241.1:n.357+8T=
XM_011536850.1:c.1226+2947T=	XP_011535152.1:n.1226+2947T=
XM_011536851.1:c.1398+8T=	XP_011535153.1:n.1398+8T=
XM_011536852.1:c.1047+8T=	XP_011535154.1:n.1047+8T=
XM_011536853.1:c.930+8T=	XP_011535155.1:n.930+8T=
XM_011536855.1:c.525+8T=	XP_011535157.1:n.525+8T=
XM_011536856.1:c.357+8T=	XP_011535158.1:n.357+8T=
XR_245695.1:n.1350+2947T=
XR_943481.1:n.1522+8T=
XM_011536851.2:c.1398+8T=	XP_011535153.1:n.1398+8T=
XM_017021379.2:c.1398+8T=	XP_016876868.1:n.1398+8T=
XM_017021380.1:c.558+8T=	XP_016876869.1:n.558+8T=
XM_024449636.1:c.357+8T=	XP_024305404.1:n.357+8T=
XR_001750382.2:n.1521+8T=
XR_001750384.2:n.1592+8T=
XR_001750385.2:n.1615+8T=
XR_001750386.2:n.1686+8T=
XR_001750387.2:n.1349+2947T=
XR_245695.2:n.1349+2947T=
NM_017799.4:c.1398+8T= MANE Select	NP_060269.3:n.1398+8T=