Canonical Allele Identifier: CA2580073887
Gene: TCOF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150392047del , CM000667.2:g.150392047del GRCh38
NC_000005.9:g.149771610del , CM000667.1:g.149771610del GRCh37
NC_000005.8:g.149751803del NCBI36
NG_011341.1:g.39409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427724.7:c.3274del ENSP00000390717.3:p.Leu1092PhefsTer?
ENST00000643257.2:c.3388del MANE Select ENSP00000493815.1:p.Leu1130PhefsTer?
ENST00000650162.1:c.3043del ENSP00000497075.1:p.Leu1015PhefsTer?
ENST00000674413.1:c.2787del
ENST00000323668.11:c.3157del ENSP00000325223.6:p.Leu1053PhefsTer?
ENST00000377797.7:c.3388del ENSP00000367028.4:p.Leu1130PhefsTer?
ENST00000427724.6:c.3274del ENSP00000390717.2:p.Leu1092PhefsTer?
ENST00000439160.6:c.3274del ENSP00000406888.2:p.Leu1092PhefsTer?
ENST00000445265.6:c.3157del ENSP00000409944.2:p.Leu1053PhefsTer?
ENST00000504761.6:c.3388del ENSP00000421655.2:p.Leu1130PhefsTer?
ENST00000506630.1:n.581del
ENST00000513346.5:c.3385del ENSP00000427484.1:p.Leu1129PhefsTer?
ENST00000514442.5:n.2326del
ENST00000515516.1:c.343-4696del ENSP00000426471.1:n.343-4696del
NM_000356.3:c.3157del NP_000347.2:p.Leu1053PhefsTer?
NM_001135243.1:c.3388del NP_001128715.1:p.Leu1130PhefsTer?
NM_001135244.1:c.3274del NP_001128716.1:p.Leu1092PhefsTer?
NM_001135245.1:c.3157del NP_001128717.1:p.Leu1053PhefsTer?
NM_001195141.1:c.3274del NP_001182070.1:p.Leu1092PhefsTer?
XM_005268502.2:c.3499del XP_005268559.1:p.Leu1167PhefsTer?
XM_005268503.2:c.3496del XP_005268560.1:p.Leu1166PhefsTer?
XM_005268504.2:c.3499del XP_005268561.1:p.Leu1167PhefsTer?
XM_005268505.2:c.3388del XP_005268562.1:p.Leu1130PhefsTer?
XM_005268506.2:c.3385del XP_005268563.1:p.Leu1129PhefsTer?
XM_005268507.2:c.3268del XP_005268564.1:p.Leu1090PhefsTer?
XM_011537678.1:c.3319del XP_011535980.1:p.Leu1107PhefsTer?
XR_427778.1:n.3503del
XR_427779.1:n.3389del
XR_427780.1:n.3392del
XM_005268502.4:c.3499del XP_005268559.1:p.Leu1167PhefsTer?
XM_005268503.4:c.3496del XP_005268560.1:p.Leu1166PhefsTer?
XM_005268504.4:c.3499del XP_005268561.1:p.Leu1167PhefsTer?
XM_005268505.4:c.3388del XP_005268562.1:p.Leu1130PhefsTer?
XM_005268506.4:c.3385del XP_005268563.1:p.Leu1129PhefsTer?
XM_005268507.4:c.3268del XP_005268564.1:p.Leu1090PhefsTer?
XM_011537678.3:c.3319del XP_011535980.1:p.Leu1107PhefsTer?
XM_017009792.2:c.3385del XP_016865281.1:p.Leu1129PhefsTer?
XM_017009793.2:c.3208del XP_016865282.1:p.Leu1070PhefsTer?
XM_017009794.2:c.3094del XP_016865283.1:p.Leu1032PhefsTer?
XR_427778.3:n.3505del
XR_427779.2:n.3391del
XR_427780.3:n.3394del
NM_000356.4:c.3157del NP_000347.2:p.Leu1053PhefsTer?
NM_001135244.2:c.3274del NP_001128716.1:p.Leu1092PhefsTer?
NM_001135245.2:c.3157del NP_001128717.1:p.Leu1053PhefsTer?
NM_001195141.2:c.3274del NP_001182070.1:p.Leu1092PhefsTer?
NM_001371623.1:c.3388del MANE Select NP_001358552.1:p.Leu1130PhefsTer?
NM_001135243.2:c.3388del NP_001128715.1:p.Leu1130PhefsTer?