Canonical Allele Identifier: CA1590917173

Gene: TCOF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150375163_150375178delinsGGTGAGGCTGGAAGCC , CM000667.2:g.150375163_150375178delinsGGTGAGGCTGGAAGCC	GRCh38
NC_000005.9:g.149754726_149754741delinsGGTGAGGCTGGAAGCC , CM000667.1:g.149754726_149754741delinsGGTGAGGCTGGAAGCC	GRCh37
NC_000005.8:g.149734919_149734934delinsGGTGAGGCTGGAAGCC	NCBI36
NG_011341.1:g.22525_22540delinsGGTGAGGCTGGAAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000513538.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000643257.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000650162.1:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
ENST00000674413.1:c.776_776+15delinsGGTGAGGCTGGAAGCC
ENST00000323668.11:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
ENST00000377797.7:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000394269.7:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000427724.6:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000439160.6:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000445265.6:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
ENST00000504761.6:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000513346.5:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
ENST00000514442.5:n.288_288+15delinsGGTGAGGCTGGAAGCC
ENST00000515035.5:n.2395_2410delinsGGTGAGGCTGGAAGCC
ENST00000515516.1:c.342+7246_342+7261delinsGGTGAGGCTGGAAGCC	ENSP00000426471.1:n.342+7246_342+7261delinsGGTGAGGCTGGAAGCC
NM_000356.3:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
NM_001008657.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135243.1:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135244.1:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135245.1:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
NM_001195141.1:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268502.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268503.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268504.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268505.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268506.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268507.2:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
XM_005268508.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268509.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_011537678.1:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XR_427778.1:n.1533_1533+15delinsGGTGAGGCTGGAAGCC
XR_427779.1:n.1533_1533+15delinsGGTGAGGCTGGAAGCC
XR_427780.1:n.1533_1533+15delinsGGTGAGGCTGGAAGCC
XM_005268502.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268503.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268504.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268505.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268506.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268507.4:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
XM_005268508.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_005268509.4:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_011537678.3:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_017009792.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_017009793.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_017009794.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
XM_017009795.2:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
XR_427778.3:n.1535_1535+15delinsGGTGAGGCTGGAAGCC
XR_427779.2:n.1535_1535+15delinsGGTGAGGCTGGAAGCC
XR_427780.3:n.1535_1535+15delinsGGTGAGGCTGGAAGCC
NM_000356.4:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
NM_001008657.3:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135244.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135245.2:c.1257_1257+15delinsGGTGAGGCTGGAAGCC
NM_001195141.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001371623.1:c.1488_1488+15delinsGGTGAGGCTGGAAGCC
NM_001135243.2:c.1488_1488+15delinsGGTGAGGCTGGAAGCC