Canonical Allele Identifier: CA389833392

Gene: TMEM260

Linked Data

• MyVariant Identifiers: chr14:g.57088417G>C (hg19) ; chr14:g.56621699G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56621699G>C , CM000676.2:g.56621699G>C	GRCh38
NC_000014.8:g.57088417G>C , CM000676.1:g.57088417G>C	GRCh37
NC_000014.7:g.56158170G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1395G>C MANE Select	ENSP00000261556.6:p.Gln465His
ENST00000261556.10:c.1395G>C	ENSP00000261556.6:p.Gln465His
ENST00000538838.5:c.1226+2936G>C	ENSP00000441934.1:n.1226+2936G>C
ENST00000539559.6:c.*305G>C	ENSP00000442602.2:n.*305G>C
ENST00000555497.5:c.*700+2936G>C	ENSP00000452065.1:n.*700+2936G>C
ENST00000555905.5:c.440+2936G>C
ENST00000556422.5:c.758+2936G>C	ENSP00000450988.1:n.758+2936G>C
ENST00000556648.1:n.862+2936G>C
NM_017799.3:c.1395G>C	NP_060269.3:p.Gln465His
XM_005267771.1:c.354G>C	XP_005267828.1:p.Gln118His
XM_006720176.1:c.555G>C	XP_006720239.1:p.Gln185His
XM_006720178.1:c.354G>C	XP_006720241.1:p.Gln118His
XM_011536850.1:c.1226+2936G>C	XP_011535152.1:n.1226+2936G>C
XM_011536851.1:c.1395G>C	XP_011535153.1:p.Gln465His
XM_011536852.1:c.1044G>C	XP_011535154.1:p.Gln348His
XM_011536853.1:c.927G>C	XP_011535155.1:p.Gln309His
XM_011536855.1:c.522G>C	XP_011535157.1:p.Gln174His
XM_011536856.1:c.354G>C	XP_011535158.1:p.Gln118His
XR_245695.1:n.1350+2936G>C
XR_943481.1:n.1519G>C
XM_011536851.2:c.1395G>C	XP_011535153.1:p.Gln465His
XM_017021379.2:c.1395G>C	XP_016876868.1:p.Gln465His
XM_017021380.1:c.555G>C	XP_016876869.1:p.Gln185His
XM_024449636.1:c.354G>C	XP_024305404.1:p.Gln118His
XR_001750382.2:n.1518G>C
XR_001750384.2:n.1589G>C
XR_001750385.2:n.1612G>C
XR_001750386.2:n.1683G>C
XR_001750387.2:n.1349+2936G>C
XR_245695.2:n.1349+2936G>C
NM_017799.4:c.1395G>C MANE Select	NP_060269.3:p.Gln465His