Canonical Allele Identifier: CA1590926016
Gene: TCOF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150393494A= , CM000667.2:g.150393494A= GRCh38
NC_000005.9:g.149773057A= , CM000667.1:g.149773057A= GRCh37
NC_000005.8:g.149753250A= NCBI36
NG_011341.1:g.40856A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427724.7:c.3609A= ENSP00000390717.3:p.Pro1203=
ENST00000643257.2:c.3726A= MANE Select ENSP00000493815.1:p.Pro1242=
ENST00000650162.1:c.3381A= ENSP00000497075.1:p.Pro1127=
ENST00000674413.1:c.3125A=
ENST00000323668.11:c.3492A= ENSP00000325223.6:p.Pro1164=
ENST00000377797.7:c.3723A= ENSP00000367028.4:p.Pro1241=
ENST00000427724.6:c.3609A= ENSP00000390717.2:p.Pro1203=
ENST00000439160.6:c.3612A= ENSP00000406888.2:p.Pro1204=
ENST00000445265.6:c.3495A= ENSP00000409944.2:p.Pro1165=
ENST00000504761.6:c.3723A= ENSP00000421655.2:p.Pro1241=
ENST00000513346.5:c.3723A= ENSP00000427484.1:p.Pro1241=
ENST00000514442.5:n.3773A=
ENST00000515516.1:c.343-3249A= ENSP00000426471.1:n.343-3249A=
NM_000356.3:c.3492A= NP_000347.2:p.Pro1164=
NM_001135243.1:c.3723A= NP_001128715.1:p.Pro1241=
NM_001135244.1:c.3612A= NP_001128716.1:p.Pro1204=
NM_001135245.1:c.3495A= NP_001128717.1:p.Pro1165=
NM_001195141.1:c.3609A= NP_001182070.1:p.Pro1203=
XM_005268502.2:c.3837A= XP_005268559.1:p.Pro1279=
XM_005268503.2:c.3834A= XP_005268560.1:p.Pro1278=
XM_005268504.2:c.3834A= XP_005268561.1:p.Pro1278=
XM_005268505.2:c.3726A= XP_005268562.1:p.Pro1242=
XM_005268506.2:c.3723A= XP_005268563.1:p.Pro1241=
XM_005268507.2:c.3606A= XP_005268564.1:p.Pro1202=
XM_011537678.1:c.3657A= XP_011535980.1:p.Pro1219=
XR_427778.1:n.3841A=
XR_427780.1:n.3730A=
XM_005268502.4:c.3837A= XP_005268559.1:p.Pro1279=
XM_005268503.4:c.3834A= XP_005268560.1:p.Pro1278=
XM_005268504.4:c.3834A= XP_005268561.1:p.Pro1278=
XM_005268505.4:c.3726A= XP_005268562.1:p.Pro1242=
XM_005268506.4:c.3723A= XP_005268563.1:p.Pro1241=
XM_005268507.4:c.3606A= XP_005268564.1:p.Pro1202=
XM_011537678.3:c.3657A= XP_011535980.1:p.Pro1219=
XM_017009792.2:c.3720A= XP_016865281.1:p.Pro1240=
XM_017009793.2:c.3546A= XP_016865282.1:p.Pro1182=
XM_017009794.2:c.3432A= XP_016865283.1:p.Pro1144=
XR_427778.3:n.3843A=
XR_427780.3:n.3732A=
NM_000356.4:c.3492A= NP_000347.2:p.Pro1164=
NM_001135244.2:c.3612A= NP_001128716.1:p.Pro1204=
NM_001135245.2:c.3495A= NP_001128717.1:p.Pro1165=
NM_001195141.2:c.3609A= NP_001182070.1:p.Pro1203=
NM_001371623.1:c.3726A= MANE Select NP_001358552.1:p.Pro1242=
NM_001135243.2:c.3723A= NP_001128715.1:p.Pro1241=