Canonical Allele Identifier: CA447157763

Gene: TCOF1

Linked Data

• MyVariant Identifiers: chr5:g.149772937T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150393374T>G , CM000667.2:g.150393374T>G	GRCh38
NC_000005.9:g.149772937T>G , CM000667.1:g.149772937T>G	GRCh37
NC_000005.8:g.149753130T>G	NCBI36
NG_011341.1:g.40736T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.3489T>G	ENSP00000390717.3:p.Ser1163=
ENST00000643257.2:c.3606T>G MANE Select	ENSP00000493815.1:p.Ser1202=
ENST00000650162.1:c.3261T>G	ENSP00000497075.1:p.Ser1087=
ENST00000674413.1:c.3005T>G
ENST00000323668.11:c.3372T>G	ENSP00000325223.6:p.Ser1124=
ENST00000377797.7:c.3603T>G	ENSP00000367028.4:p.Ser1201=
ENST00000427724.6:c.3489T>G	ENSP00000390717.2:p.Ser1163=
ENST00000439160.6:c.3492T>G	ENSP00000406888.2:p.Ser1164=
ENST00000445265.6:c.3375T>G	ENSP00000409944.2:p.Ser1125=
ENST00000504761.6:c.3603T>G	ENSP00000421655.2:p.Ser1201=
ENST00000513346.5:c.3603T>G	ENSP00000427484.1:p.Ser1201=
ENST00000514442.5:n.3653T>G
ENST00000515516.1:c.343-3369T>G	ENSP00000426471.1:n.343-3369T>G
NM_000356.3:c.3372T>G	NP_000347.2:p.Ser1124=
NM_001135243.1:c.3603T>G	NP_001128715.1:p.Ser1201=
NM_001135244.1:c.3492T>G	NP_001128716.1:p.Ser1164=
NM_001135245.1:c.3375T>G	NP_001128717.1:p.Ser1125=
NM_001195141.1:c.3489T>G	NP_001182070.1:p.Ser1163=
XM_005268502.2:c.3717T>G	XP_005268559.1:p.Ser1239=
XM_005268503.2:c.3714T>G	XP_005268560.1:p.Ser1238=
XM_005268504.2:c.3714T>G	XP_005268561.1:p.Ser1238=
XM_005268505.2:c.3606T>G	XP_005268562.1:p.Ser1202=
XM_005268506.2:c.3603T>G	XP_005268563.1:p.Ser1201=
XM_005268507.2:c.3486T>G	XP_005268564.1:p.Ser1162=
XM_011537678.1:c.3537T>G	XP_011535980.1:p.Ser1179=
XR_427778.1:n.3721T>G
XR_427780.1:n.3610T>G
XM_005268502.4:c.3717T>G	XP_005268559.1:p.Ser1239=
XM_005268503.4:c.3714T>G	XP_005268560.1:p.Ser1238=
XM_005268504.4:c.3714T>G	XP_005268561.1:p.Ser1238=
XM_005268505.4:c.3606T>G	XP_005268562.1:p.Ser1202=
XM_005268506.4:c.3603T>G	XP_005268563.1:p.Ser1201=
XM_005268507.4:c.3486T>G	XP_005268564.1:p.Ser1162=
XM_011537678.3:c.3537T>G	XP_011535980.1:p.Ser1179=
XM_017009792.2:c.3600T>G	XP_016865281.1:p.Ser1200=
XM_017009793.2:c.3426T>G	XP_016865282.1:p.Ser1142=
XM_017009794.2:c.3312T>G	XP_016865283.1:p.Ser1104=
XR_427778.3:n.3723T>G
XR_427780.3:n.3612T>G
NM_000356.4:c.3372T>G	NP_000347.2:p.Ser1124=
NM_001135244.2:c.3492T>G	NP_001128716.1:p.Ser1164=
NM_001135245.2:c.3375T>G	NP_001128717.1:p.Ser1125=
NM_001195141.2:c.3489T>G	NP_001182070.1:p.Ser1163=
NM_001371623.1:c.3606T>G MANE Select	NP_001358552.1:p.Ser1202=
NM_001135243.2:c.3603T>G	NP_001128715.1:p.Ser1201=