Canonical Allele Identifier: CA361743634
Community Standard Title: NM_001371623.1(TCOF1):c.4243A>T (p.Lys1415Ter)
Gene: TCOF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150396740A>T , CM000667.2:g.150396740A>T GRCh38
NC_000005.9:g.149776303A>T , CM000667.1:g.149776303A>T GRCh37
NC_000005.8:g.149756496A>T NCBI36
NG_011341.1:g.44102A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001371623.1:c.4243A>T MANE Select NP_001358552.1:p.Lys1415Ter
ENST00000643257.2:c.4243A>T MANE Select ENSP00000493815.1:p.Lys1415Ter
NM_000356.3:c.4009A>T NP_000347.2:p.Lys1337Ter
NM_000356.4:c.4009A>T NP_000347.2:p.Lys1337Ter
NM_001135243.1:c.4240A>T NP_001128715.1:p.Lys1414Ter
NM_001135243.2:c.4240A>T NP_001128715.1:p.Lys1414Ter
NM_001135244.1:c.4129A>T NP_001128716.1:p.Lys1377Ter
NM_001135244.2:c.4129A>T NP_001128716.1:p.Lys1377Ter
NM_001135245.1:c.4012A>T NP_001128717.1:p.Lys1338Ter
NM_001135245.2:c.4012A>T NP_001128717.1:p.Lys1338Ter
NM_001195141.1:c.4126A>T NP_001182070.1:p.Lys1376Ter
NM_001195141.2:c.4126A>T NP_001182070.1:p.Lys1376Ter
ENST00000323668.11:c.4009A>T ENSP00000325223.6:p.Lys1337Ter
ENST00000377797.7:c.4240A>T ENSP00000367028.4:p.Lys1414Ter
ENST00000427724.6:c.4126A>T ENSP00000390717.2:p.Lys1376Ter
ENST00000427724.7:c.4126A>T ENSP00000390717.3:p.Lys1376Ter
ENST00000439160.6:c.4129A>T ENSP00000406888.2:p.Lys1377Ter
ENST00000445265.6:c.4012A>T ENSP00000409944.2:p.Lys1338Ter
ENST00000504761.6:c.4240A>T ENSP00000421655.2:p.Lys1414Ter
ENST00000513346.5:c.4240A>T ENSP00000427484.1:p.Lys1414Ter
ENST00000515516.1:c.343-3A>T ENSP00000426471.1:n.343-3A>T
ENST00000650162.1:c.3898A>T ENSP00000497075.1:p.Lys1300Ter
ENST00000674413.1:c.3642A>T
XM_005268502.2:c.4354A>T XP_005268559.1:p.Lys1452Ter
XM_005268502.4:c.4354A>T XP_005268559.1:p.Lys1452Ter
XM_005268503.2:c.4351A>T XP_005268560.1:p.Lys1451Ter
XM_005268503.4:c.4351A>T XP_005268560.1:p.Lys1451Ter
XM_005268504.2:c.4351A>T XP_005268561.1:p.Lys1451Ter
XM_005268504.4:c.4351A>T XP_005268561.1:p.Lys1451Ter
XM_005268505.2:c.4243A>T XP_005268562.1:p.Lys1415Ter
XM_005268505.4:c.4243A>T XP_005268562.1:p.Lys1415Ter
XM_005268506.2:c.4240A>T XP_005268563.1:p.Lys1414Ter
XM_005268506.4:c.4240A>T XP_005268563.1:p.Lys1414Ter
XM_005268507.2:c.4123A>T XP_005268564.1:p.Lys1375Ter
XM_005268507.4:c.4123A>T XP_005268564.1:p.Lys1375Ter
XM_011537678.1:c.4174A>T XP_011535980.1:p.Lys1392Ter
XM_011537678.3:c.4174A>T XP_011535980.1:p.Lys1392Ter
XM_017009792.2:c.4237A>T XP_016865281.1:p.Lys1413Ter
XM_017009793.2:c.4063A>T XP_016865282.1:p.Lys1355Ter
XM_017009794.2:c.3949A>T XP_016865283.1:p.Lys1317Ter
XR_427778.3:n.4360A>T
XR_427780.3:n.4249A>T