Canonical Allele Identifier: CA2675991677

Gene: TCOF1

Linked Data

• gnomAD v4: 5-150379449-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150379451dup , CM000667.2:g.150379451dup	GRCh38
NC_000005.9:g.149759014dup , CM000667.1:g.149759014dup	GRCh37
NC_000005.8:g.149739207dup	NCBI36
NG_011341.1:g.26813dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000427724.7:c.2658+43dup	ENSP00000390717.3:n.2658+43dup
ENST00000513538.2:c.2658+43dup	ENSP00000422567.2:n.2658+43dup
ENST00000643257.2:c.2658+43dup MANE Select	ENSP00000493815.1:n.2658+43dup
ENST00000650162.1:c.2427+43dup	ENSP00000497075.1:n.2427+43dup
ENST00000674413.1:c.1946+43dup
ENST00000323668.11:c.2427+43dup	ENSP00000325223.6:n.2427+43dup
ENST00000377797.7:c.2658+43dup	ENSP00000367028.4:n.2658+43dup
ENST00000394269.7:c.2658+43dup	ENSP00000377811.3:n.2658+43dup
ENST00000427724.6:c.2658+43dup	ENSP00000390717.2:n.2658+43dup
ENST00000439160.6:c.2658+43dup	ENSP00000406888.2:n.2658+43dup
ENST00000445265.6:c.2427+43dup	ENSP00000409944.2:n.2427+43dup
ENST00000504761.6:c.2658+43dup	ENSP00000421655.2:n.2658+43dup
ENST00000506063.1:n.413+43dup
ENST00000506767.1:c.133+43dup
ENST00000513346.5:c.2658+43dup	ENSP00000427484.1:n.2658+43dup
ENST00000514442.5:n.1458+43dup
ENST00000515035.5:n.3912+43dup
ENST00000515516.1:c.342+11534dup	ENSP00000426471.1:n.342+11534dup
NM_000356.3:c.2427+43dup	NP_000347.2:n.2427+43dup
NM_001008657.2:c.2658+43dup	NP_001008657.1:n.2658+43dup
NM_001135243.1:c.2658+43dup	NP_001128715.1:n.2658+43dup
NM_001135244.1:c.2658+43dup	NP_001128716.1:n.2658+43dup
NM_001135245.1:c.2427+43dup	NP_001128717.1:n.2427+43dup
NM_001195141.1:c.2658+43dup	NP_001182070.1:n.2658+43dup
XM_005268502.2:c.2658+43dup	XP_005268559.1:n.2658+43dup
XM_005268503.2:c.2658+43dup	XP_005268560.1:n.2658+43dup
XM_005268504.2:c.2658+43dup	XP_005268561.1:n.2658+43dup
XM_005268505.2:c.2658+43dup	XP_005268562.1:n.2658+43dup
XM_005268506.2:c.2658+43dup	XP_005268563.1:n.2658+43dup
XM_005268507.2:c.2427+43dup	XP_005268564.1:n.2427+43dup
XM_005268508.2:c.2658+43dup	XP_005268565.1:n.2658+43dup
XM_005268509.2:c.2658+43dup	XP_005268566.1:n.2658+43dup
XM_011537678.1:c.2479-81dup	XP_011535980.1:n.2479-81dup
XR_427778.1:n.2703+43dup
XR_427779.1:n.2703+43dup
XR_427780.1:n.2703+43dup
XM_005268502.4:c.2658+43dup	XP_005268559.1:n.2658+43dup
XM_005268503.4:c.2658+43dup	XP_005268560.1:n.2658+43dup
XM_005268504.4:c.2658+43dup	XP_005268561.1:n.2658+43dup
XM_005268505.4:c.2658+43dup	XP_005268562.1:n.2658+43dup
XM_005268506.4:c.2658+43dup	XP_005268563.1:n.2658+43dup
XM_005268507.4:c.2427+43dup	XP_005268564.1:n.2427+43dup
XM_005268508.4:c.2658+43dup	XP_005268565.1:n.2658+43dup
XM_005268509.4:c.2658+43dup	XP_005268566.1:n.2658+43dup
XM_011537678.3:c.2479-81dup	XP_011535980.1:n.2479-81dup
XM_017009792.2:c.2658+43dup	XP_016865281.1:n.2658+43dup
XM_017009793.2:c.2479-81dup	XP_016865282.1:n.2479-81dup
XM_017009794.2:c.2479-81dup	XP_016865283.1:n.2479-81dup
XM_017009795.2:c.2427+43dup	XP_016865284.1:n.2427+43dup
XR_427778.3:n.2705+43dup
XR_427779.2:n.2705+43dup
XR_427780.3:n.2705+43dup
NM_000356.4:c.2427+43dup	NP_000347.2:n.2427+43dup
NM_001008657.3:c.2658+43dup	NP_001008657.1:n.2658+43dup
NM_001135244.2:c.2658+43dup	NP_001128716.1:n.2658+43dup
NM_001135245.2:c.2427+43dup	NP_001128717.1:n.2427+43dup
NM_001195141.2:c.2658+43dup	NP_001182070.1:n.2658+43dup
NM_001371623.1:c.2658+43dup MANE Select	NP_001358552.1:n.2658+43dup
NM_001135243.2:c.2658+43dup	NP_001128715.1:n.2658+43dup