Canonical Allele Identifier: CA361741411

Gene: TCOF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150396353C>T , CM000667.2:g.150396353C>T	GRCh38
NC_000005.9:g.149775916C>T , CM000667.1:g.149775916C>T	GRCh37
NC_000005.8:g.149756109C>T	NCBI36
NG_011341.1:g.43715C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001371623.1:c.3856C>T MANE Select	NP_001358552.1:p.Gln1286Ter
ENST00000643257.2:c.3856C>T MANE Select	ENSP00000493815.1:p.Gln1286Ter
NM_000356.3:c.3622C>T	NP_000347.2:p.Gln1208Ter
NM_000356.4:c.3622C>T	NP_000347.2:p.Gln1208Ter
NM_001135243.1:c.3853C>T	NP_001128715.1:p.Gln1285Ter
NM_001135243.2:c.3853C>T	NP_001128715.1:p.Gln1285Ter
NM_001135244.1:c.3742C>T	NP_001128716.1:p.Gln1248Ter
NM_001135244.2:c.3742C>T	NP_001128716.1:p.Gln1248Ter
NM_001135245.1:c.3625C>T	NP_001128717.1:p.Gln1209Ter
NM_001135245.2:c.3625C>T	NP_001128717.1:p.Gln1209Ter
NM_001195141.1:c.3739C>T	NP_001182070.1:p.Gln1247Ter
NM_001195141.2:c.3739C>T	NP_001182070.1:p.Gln1247Ter
ENST00000323668.11:c.3622C>T	ENSP00000325223.6:p.Gln1208Ter
ENST00000377797.7:c.3853C>T	ENSP00000367028.4:p.Gln1285Ter
ENST00000427724.6:c.3739C>T	ENSP00000390717.2:p.Gln1247Ter
ENST00000427724.7:c.3739C>T	ENSP00000390717.3:p.Gln1247Ter
ENST00000439160.6:c.3742C>T	ENSP00000406888.2:p.Gln1248Ter
ENST00000445265.6:c.3625C>T	ENSP00000409944.2:p.Gln1209Ter
ENST00000504761.6:c.3853C>T	ENSP00000421655.2:p.Gln1285Ter
ENST00000513346.5:c.3853C>T	ENSP00000427484.1:p.Gln1285Ter
ENST00000515516.1:c.343-390C>T	ENSP00000426471.1:n.343-390C>T
ENST00000650162.1:c.3511C>T	ENSP00000497075.1:p.Gln1171Ter
ENST00000674413.1:c.3255C>T
XM_005268502.2:c.3967C>T	XP_005268559.1:p.Gln1323Ter
XM_005268502.4:c.3967C>T	XP_005268559.1:p.Gln1323Ter
XM_005268503.2:c.3964C>T	XP_005268560.1:p.Gln1322Ter
XM_005268503.4:c.3964C>T	XP_005268560.1:p.Gln1322Ter
XM_005268504.2:c.3964C>T	XP_005268561.1:p.Gln1322Ter
XM_005268504.4:c.3964C>T	XP_005268561.1:p.Gln1322Ter
XM_005268505.2:c.3856C>T	XP_005268562.1:p.Gln1286Ter
XM_005268505.4:c.3856C>T	XP_005268562.1:p.Gln1286Ter
XM_005268506.2:c.3853C>T	XP_005268563.1:p.Gln1285Ter
XM_005268506.4:c.3853C>T	XP_005268563.1:p.Gln1285Ter
XM_005268507.2:c.3736C>T	XP_005268564.1:p.Gln1246Ter
XM_005268507.4:c.3736C>T	XP_005268564.1:p.Gln1246Ter
XM_011537678.1:c.3787C>T	XP_011535980.1:p.Gln1263Ter
XM_011537678.3:c.3787C>T	XP_011535980.1:p.Gln1263Ter
XM_017009792.2:c.3850C>T	XP_016865281.1:p.Gln1284Ter
XM_017009793.2:c.3676C>T	XP_016865282.1:p.Gln1226Ter
XM_017009794.2:c.3562C>T	XP_016865283.1:p.Gln1188Ter
XR_427778.3:n.3973C>T
XR_427780.3:n.3862C>T