Canonical Allele Identifier: CA252945
Gene: TCOF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150375489_150375490del , CM000667.2:g.150375489_150375490del GRCh38
NC_000005.9:g.149755052_149755053del , CM000667.1:g.149755052_149755053del GRCh37
NC_000005.8:g.149735245_149735246del NCBI36
NG_011341.1:g.22851_22852del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427724.7:c.1639_1640del ENSP00000390717.3:p.Ser547GlnfsTer2
ENST00000513538.2:c.1639_1640del ENSP00000422567.2:p.Ser547GlnfsTer2
ENST00000643257.2:c.1639_1640del MANE Select ENSP00000493815.1:p.Ser547GlnfsTer2
ENST00000650162.1:c.1408_1409del ENSP00000497075.1:p.Ser470GlnfsTer2
ENST00000674413.1:c.927_928del
ENST00000323668.11:c.1408_1409del ENSP00000325223.6:p.Ser470GlnfsTer2
ENST00000377797.7:c.1639_1640del ENSP00000367028.4:p.Ser547GlnfsTer2
ENST00000394269.7:c.1639_1640del ENSP00000377811.3:p.Ser547GlnfsTer2
ENST00000427724.6:c.1639_1640del ENSP00000390717.2:p.Ser547GlnfsTer2
ENST00000439160.6:c.1639_1640del ENSP00000406888.2:p.Ser547GlnfsTer2
ENST00000445265.6:c.1408_1409del ENSP00000409944.2:p.Ser470GlnfsTer2
ENST00000504761.6:c.1639_1640del ENSP00000421655.2:p.Ser547GlnfsTer2
ENST00000513346.5:c.1639_1640del ENSP00000427484.1:p.Ser547GlnfsTer2
ENST00000514442.5:n.439_440del
ENST00000515035.5:n.2721_2722del
ENST00000515516.1:c.342+7572_342+7573del ENSP00000426471.1:n.342+7572_342+7573del
NM_000356.3:c.1408_1409del NP_000347.2:p.Ser470GlnfsTer2
NM_001008657.2:c.1639_1640del NP_001008657.1:p.Ser547GlnfsTer2
NM_001135243.1:c.1639_1640del NP_001128715.1:p.Ser547GlnfsTer2
NM_001135244.1:c.1639_1640del NP_001128716.1:p.Ser547GlnfsTer2
NM_001135245.1:c.1408_1409del NP_001128717.1:p.Ser470GlnfsTer2
NM_001195141.1:c.1639_1640del NP_001182070.1:p.Ser547GlnfsTer2
XM_005268502.2:c.1639_1640del XP_005268559.1:p.Ser547GlnfsTer2
XM_005268503.2:c.1639_1640del XP_005268560.1:p.Ser547GlnfsTer2
XM_005268504.2:c.1639_1640del XP_005268561.1:p.Ser547GlnfsTer2
XM_005268505.2:c.1639_1640del XP_005268562.1:p.Ser547GlnfsTer2
XM_005268506.2:c.1639_1640del XP_005268563.1:p.Ser547GlnfsTer2
XM_005268507.2:c.1408_1409del XP_005268564.1:p.Ser470GlnfsTer2
XM_005268508.2:c.1639_1640del XP_005268565.1:p.Ser547GlnfsTer2
XM_005268509.2:c.1639_1640del XP_005268566.1:p.Ser547GlnfsTer2
XM_011537678.1:c.1639_1640del XP_011535980.1:p.Ser547GlnfsTer2
XR_427778.1:n.1684_1685del
XR_427779.1:n.1684_1685del
XR_427780.1:n.1684_1685del
XM_005268502.4:c.1639_1640del XP_005268559.1:p.Ser547GlnfsTer2
XM_005268503.4:c.1639_1640del XP_005268560.1:p.Ser547GlnfsTer2
XM_005268504.4:c.1639_1640del XP_005268561.1:p.Ser547GlnfsTer2
XM_005268505.4:c.1639_1640del XP_005268562.1:p.Ser547GlnfsTer2
XM_005268506.4:c.1639_1640del XP_005268563.1:p.Ser547GlnfsTer2
XM_005268507.4:c.1408_1409del XP_005268564.1:p.Ser470GlnfsTer2
XM_005268508.4:c.1639_1640del XP_005268565.1:p.Ser547GlnfsTer2
XM_005268509.4:c.1639_1640del XP_005268566.1:p.Ser547GlnfsTer2
XM_011537678.3:c.1639_1640del XP_011535980.1:p.Ser547GlnfsTer2
XM_017009792.2:c.1639_1640del XP_016865281.1:p.Ser547GlnfsTer2
XM_017009793.2:c.1639_1640del XP_016865282.1:p.Ser547GlnfsTer2
XM_017009794.2:c.1639_1640del XP_016865283.1:p.Ser547GlnfsTer2
XM_017009795.2:c.1408_1409del XP_016865284.1:p.Ser470GlnfsTer2
XR_427778.3:n.1686_1687del
XR_427779.2:n.1686_1687del
XR_427780.3:n.1686_1687del
NM_000356.4:c.1408_1409del NP_000347.2:p.Ser470GlnfsTer2
NM_001008657.3:c.1639_1640del NP_001008657.1:p.Ser547GlnfsTer2
NM_001135244.2:c.1639_1640del NP_001128716.1:p.Ser547GlnfsTer2
NM_001135245.2:c.1408_1409del NP_001128717.1:p.Ser470GlnfsTer2
NM_001195141.2:c.1639_1640del NP_001182070.1:p.Ser547GlnfsTer2
NM_001371623.1:c.1639_1640del MANE Select NP_001358552.1:p.Ser547GlnfsTer2
NM_001135243.2:c.1639_1640del NP_001128715.1:p.Ser547GlnfsTer2