Canonical Allele Identifier: CA7199794

Gene: TMEM260

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56605651C>T , CM000676.2:g.56605651C>T	GRCh38
NC_000014.8:g.57072369C>T , CM000676.1:g.57072369C>T	GRCh37
NC_000014.7:g.56142122C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017799.4:c.604C>T MANE Select	NP_060269.3:p.Pro202Ser
ENST00000261556.11:c.604C>T MANE Select	ENSP00000261556.6:p.Pro202Ser
NM_017799.3:c.604C>T	NP_060269.3:p.Pro202Ser
ENST00000261556.10:c.604C>T	ENSP00000261556.6:p.Pro202Ser
ENST00000538838.5:c.604C>T	ENSP00000441934.1:p.Pro202Ser
ENST00000539559.6:c.604C>T	ENSP00000442602.2:p.Pro202Ser
ENST00000555497.5:c.*78C>T	ENSP00000452065.1:n.*78C>T
ENST00000556079.1:n.480C>T
ENST00000556422.5:c.136C>T	ENSP00000450988.1:p.Pro46Ser
ENST00000556929.5:c.140C>T
ENST00000557626.5:n.688C>T
ENST00000557657.5:n.694C>T
XM_005267771.1:c.-323C>T	XP_005267828.1:n.-323C>T
XM_006720176.1:c.-237C>T	XP_006720239.1:n.-237C>T
XM_006720177.2:c.604C>T	XP_006720240.1:p.Pro202Ser
XM_006720178.1:c.-323C>T	XP_006720241.1:n.-323C>T
XM_011536850.1:c.604C>T	XP_011535152.1:p.Pro202Ser
XM_011536851.1:c.604C>T	XP_011535153.1:p.Pro202Ser
XM_011536851.2:c.604C>T	XP_011535153.1:p.Pro202Ser
XM_011536852.1:c.253C>T	XP_011535154.1:p.Pro85Ser
XM_011536853.1:c.136C>T	XP_011535155.1:p.Pro46Ser
XM_011536854.1:c.604C>T	XP_011535156.1:p.Pro202Ser
XM_017021379.2:c.604C>T	XP_016876868.1:p.Pro202Ser
XM_017021380.1:c.-237C>T	XP_016876869.1:n.-237C>T
XM_024449636.1:c.-323C>T	XP_024305404.1:n.-323C>T
XR_001750382.2:n.727C>T
XR_001750384.2:n.727C>T
XR_001750385.2:n.727C>T
XR_001750386.2:n.727C>T
XR_001750387.2:n.727C>T
XR_245695.1:n.728C>T
XR_245695.2:n.727C>T
XR_943481.1:n.728C>T