Canonical Allele Identifier: CA389833388

Gene: TMEM260

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000261556.11:c.1393C>A MANE Select	ENSP00000261556.6:p.Gln465Lys
ENST00000261556.10:c.1393C>A	ENSP00000261556.6:p.Gln465Lys
ENST00000538838.5:c.1226+2934C>A	ENSP00000441934.1:n.1226+2934C>A
ENST00000539559.6:c.*303C>A	ENSP00000442602.2:n.*303C>A
ENST00000555497.5:c.*700+2934C>A	ENSP00000452065.1:n.*700+2934C>A
ENST00000555905.5:c.440+2934C>A
ENST00000556422.5:c.758+2934C>A	ENSP00000450988.1:n.758+2934C>A
ENST00000556648.1:n.862+2934C>A
NM_017799.3:c.1393C>A	NP_060269.3:p.Gln465Lys
XM_005267771.1:c.352C>A	XP_005267828.1:p.Gln118Lys
XM_006720176.1:c.553C>A	XP_006720239.1:p.Gln185Lys
XM_006720178.1:c.352C>A	XP_006720241.1:p.Gln118Lys
XM_011536850.1:c.1226+2934C>A	XP_011535152.1:n.1226+2934C>A
XM_011536851.1:c.1393C>A	XP_011535153.1:p.Gln465Lys
XM_011536852.1:c.1042C>A	XP_011535154.1:p.Gln348Lys
XM_011536853.1:c.925C>A	XP_011535155.1:p.Gln309Lys
XM_011536855.1:c.520C>A	XP_011535157.1:p.Gln174Lys
XM_011536856.1:c.352C>A	XP_011535158.1:p.Gln118Lys
XR_245695.1:n.1350+2934C>A
XR_943481.1:n.1517C>A
XM_011536851.2:c.1393C>A	XP_011535153.1:p.Gln465Lys
XM_017021379.2:c.1393C>A	XP_016876868.1:p.Gln465Lys
XM_017021380.1:c.553C>A	XP_016876869.1:p.Gln185Lys
XM_024449636.1:c.352C>A	XP_024305404.1:p.Gln118Lys
XR_001750382.2:n.1516C>A
XR_001750384.2:n.1587C>A
XR_001750385.2:n.1610C>A
XR_001750386.2:n.1681C>A
XR_001750387.2:n.1349+2934C>A
XR_245695.2:n.1349+2934C>A
NM_017799.4:c.1393C>A MANE Select	NP_060269.3:p.Gln465Lys