Canonical Allele Identifier: CA2139044717

Gene: TMEM260

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56621702A= , CM000676.2:g.56621702A=	GRCh38
NC_000014.8:g.57088420A= , CM000676.1:g.57088420A=	GRCh37
NC_000014.7:g.56158173A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1398A= MANE Select	ENSP00000261556.6:p.Glu466=
ENST00000261556.10:c.1398A=	ENSP00000261556.6:p.Glu466=
ENST00000538838.5:c.1226+2939A=	ENSP00000441934.1:n.1226+2939A=
ENST00000539559.6:c.*308A=	ENSP00000442602.2:n.*308A=
ENST00000555497.5:c.*700+2939A=	ENSP00000452065.1:n.*700+2939A=
ENST00000555905.5:c.440+2939A=
ENST00000556422.5:c.758+2939A=	ENSP00000450988.1:n.758+2939A=
ENST00000556648.1:n.862+2939A=
NM_017799.3:c.1398A=	NP_060269.3:p.Glu466=
XM_005267771.1:c.357A=	XP_005267828.1:p.Glu119=
XM_006720176.1:c.558A=	XP_006720239.1:p.Glu186=
XM_006720178.1:c.357A=	XP_006720241.1:p.Glu119=
XM_011536850.1:c.1226+2939A=	XP_011535152.1:n.1226+2939A=
XM_011536851.1:c.1398A=	XP_011535153.1:p.Glu466=
XM_011536852.1:c.1047A=	XP_011535154.1:p.Glu349=
XM_011536853.1:c.930A=	XP_011535155.1:p.Glu310=
XM_011536855.1:c.525A=	XP_011535157.1:p.Glu175=
XM_011536856.1:c.357A=	XP_011535158.1:p.Glu119=
XR_245695.1:n.1350+2939A=
XR_943481.1:n.1522A=
XM_011536851.2:c.1398A=	XP_011535153.1:p.Glu466=
XM_017021379.2:c.1398A=	XP_016876868.1:p.Glu466=
XM_017021380.1:c.558A=	XP_016876869.1:p.Glu186=
XM_024449636.1:c.357A=	XP_024305404.1:p.Glu119=
XR_001750382.2:n.1521A=
XR_001750384.2:n.1592A=
XR_001750385.2:n.1615A=
XR_001750386.2:n.1686A=
XR_001750387.2:n.1349+2939A=
XR_245695.2:n.1349+2939A=
NM_017799.4:c.1398A= MANE Select	NP_060269.3:p.Glu466=