Canonical Allele Identifier: CA1590926031

Gene: TCOF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150393534_150393537delinsATGT , CM000667.2:g.150393534_150393537delinsATGT	GRCh38
NC_000005.9:g.149773097_149773100delinsATGT , CM000667.1:g.149773097_149773100delinsATGT	GRCh37
NC_000005.8:g.149753290_149753293delinsATGT	NCBI36
NG_011341.1:g.40896_40899delinsATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000427724.7:c.3649_3652delinsATGT	ENSP00000390717.3:p.Met1217=
ENST00000643257.2:c.3766_3769delinsATGT MANE Select	ENSP00000493815.1:p.Met1256=
ENST00000650162.1:c.3421_3424delinsATGT	ENSP00000497075.1:p.Met1141=
ENST00000674413.1:c.3165_3168delinsATGT
ENST00000323668.11:c.3532_3535delinsATGT	ENSP00000325223.6:p.Met1178=
ENST00000377797.7:c.3763_3766delinsATGT	ENSP00000367028.4:p.Met1255=
ENST00000427724.6:c.3649_3652delinsATGT	ENSP00000390717.2:p.Met1217=
ENST00000439160.6:c.3652_3655delinsATGT	ENSP00000406888.2:p.Met1218=
ENST00000445265.6:c.3535_3538delinsATGT	ENSP00000409944.2:p.Met1179=
ENST00000504761.6:c.3763_3766delinsATGT	ENSP00000421655.2:p.Met1255=
ENST00000513346.5:c.3763_3766delinsATGT	ENSP00000427484.1:p.Met1255=
ENST00000514442.5:n.3813_3816delinsATGT
ENST00000515516.1:c.343-3209_343-3206delinsATGT	ENSP00000426471.1:n.343-3209_343-3206deli...
NM_000356.3:c.3532_3535delinsATGT	NP_000347.2:p.Met1178=
NM_001135243.1:c.3763_3766delinsATGT	NP_001128715.1:p.Met1255=
NM_001135244.1:c.3652_3655delinsATGT	NP_001128716.1:p.Met1218=
NM_001135245.1:c.3535_3538delinsATGT	NP_001128717.1:p.Met1179=
NM_001195141.1:c.3649_3652delinsATGT	NP_001182070.1:p.Met1217=
XM_005268502.2:c.3877_3880delinsATGT	XP_005268559.1:p.Met1293=
XM_005268503.2:c.3874_3877delinsATGT	XP_005268560.1:p.Met1292=
XM_005268504.2:c.3874_3877delinsATGT	XP_005268561.1:p.Met1292=
XM_005268505.2:c.3766_3769delinsATGT	XP_005268562.1:p.Met1256=
XM_005268506.2:c.3763_3766delinsATGT	XP_005268563.1:p.Met1255=
XM_005268507.2:c.3646_3649delinsATGT	XP_005268564.1:p.Met1216=
XM_011537678.1:c.3697_3700delinsATGT	XP_011535980.1:p.Met1233=
XM_005268502.4:c.3877_3880delinsATGT	XP_005268559.1:p.Met1293=
XM_005268503.4:c.3874_3877delinsATGT	XP_005268560.1:p.Met1292=
XM_005268504.4:c.3874_3877delinsATGT	XP_005268561.1:p.Met1292=
XM_005268505.4:c.3766_3769delinsATGT	XP_005268562.1:p.Met1256=
XM_005268506.4:c.3763_3766delinsATGT	XP_005268563.1:p.Met1255=
XM_005268507.4:c.3646_3649delinsATGT	XP_005268564.1:p.Met1216=
XM_011537678.3:c.3697_3700delinsATGT	XP_011535980.1:p.Met1233=
XM_017009792.2:c.3760_3763delinsATGT	XP_016865281.1:p.Met1254=
XM_017009793.2:c.3586_3589delinsATGT	XP_016865282.1:p.Met1196=
XM_017009794.2:c.3472_3475delinsATGT	XP_016865283.1:p.Met1158=
XR_427778.3:n.3883_3886delinsATGT
XR_427780.3:n.3772_3775delinsATGT
NM_000356.4:c.3532_3535delinsATGT	NP_000347.2:p.Met1178=
NM_001135244.2:c.3652_3655delinsATGT	NP_001128716.1:p.Met1218=
NM_001135245.2:c.3535_3538delinsATGT	NP_001128717.1:p.Met1179=
NM_001195141.2:c.3649_3652delinsATGT	NP_001182070.1:p.Met1217=
NM_001371623.1:c.3766_3769delinsATGT MANE Select	NP_001358552.1:p.Met1256=
NM_001135243.2:c.3763_3766delinsATGT	NP_001128715.1:p.Met1255=