Canonical Allele Identifier: CA389833389

Gene: TMEM260

Linked Data

• MyVariant Identifiers: chr14:g.57088415C>G (hg19) ; chr14:g.56621697C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56621697C>G , CM000676.2:g.56621697C>G	GRCh38
NC_000014.8:g.57088415C>G , CM000676.1:g.57088415C>G	GRCh37
NC_000014.7:g.56158168C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1393C>G MANE Select	ENSP00000261556.6:p.Gln465Glu
ENST00000261556.10:c.1393C>G	ENSP00000261556.6:p.Gln465Glu
ENST00000538838.5:c.1226+2934C>G	ENSP00000441934.1:n.1226+2934C>G
ENST00000539559.6:c.*303C>G	ENSP00000442602.2:n.*303C>G
ENST00000555497.5:c.*700+2934C>G	ENSP00000452065.1:n.*700+2934C>G
ENST00000555905.5:c.440+2934C>G
ENST00000556422.5:c.758+2934C>G	ENSP00000450988.1:n.758+2934C>G
ENST00000556648.1:n.862+2934C>G
NM_017799.3:c.1393C>G	NP_060269.3:p.Gln465Glu
XM_005267771.1:c.352C>G	XP_005267828.1:p.Gln118Glu
XM_006720176.1:c.553C>G	XP_006720239.1:p.Gln185Glu
XM_006720178.1:c.352C>G	XP_006720241.1:p.Gln118Glu
XM_011536850.1:c.1226+2934C>G	XP_011535152.1:n.1226+2934C>G
XM_011536851.1:c.1393C>G	XP_011535153.1:p.Gln465Glu
XM_011536852.1:c.1042C>G	XP_011535154.1:p.Gln348Glu
XM_011536853.1:c.925C>G	XP_011535155.1:p.Gln309Glu
XM_011536855.1:c.520C>G	XP_011535157.1:p.Gln174Glu
XM_011536856.1:c.352C>G	XP_011535158.1:p.Gln118Glu
XR_245695.1:n.1350+2934C>G
XR_943481.1:n.1517C>G
XM_011536851.2:c.1393C>G	XP_011535153.1:p.Gln465Glu
XM_017021379.2:c.1393C>G	XP_016876868.1:p.Gln465Glu
XM_017021380.1:c.553C>G	XP_016876869.1:p.Gln185Glu
XM_024449636.1:c.352C>G	XP_024305404.1:p.Gln118Glu
XR_001750382.2:n.1516C>G
XR_001750384.2:n.1587C>G
XR_001750385.2:n.1610C>G
XR_001750386.2:n.1681C>G
XR_001750387.2:n.1349+2934C>G
XR_245695.2:n.1349+2934C>G
NM_017799.4:c.1393C>G MANE Select	NP_060269.3:p.Gln465Glu