Canonical Allele Identifier: CA361739781

Gene: TCOF1

Linked Data

• MyVariant Identifiers: chr5:g.149773074C>T (hg19) ; chr5:g.150393511C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150393511C>T , CM000667.2:g.150393511C>T	GRCh38
NC_000005.9:g.149773074C>T , CM000667.1:g.149773074C>T	GRCh37
NC_000005.8:g.149753267C>T	NCBI36
NG_011341.1:g.40873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.3626C>T	ENSP00000390717.3:p.Ala1209Val
ENST00000643257.2:c.3743C>T MANE Select	ENSP00000493815.1:p.Ala1248Val
ENST00000650162.1:c.3398C>T	ENSP00000497075.1:p.Ala1133Val
ENST00000674413.1:c.3142C>T
ENST00000323668.11:c.3509C>T	ENSP00000325223.6:p.Ala1170Val
ENST00000377797.7:c.3740C>T	ENSP00000367028.4:p.Ala1247Val
ENST00000427724.6:c.3626C>T	ENSP00000390717.2:p.Ala1209Val
ENST00000439160.6:c.3629C>T	ENSP00000406888.2:p.Ala1210Val
ENST00000445265.6:c.3512C>T	ENSP00000409944.2:p.Ala1171Val
ENST00000504761.6:c.3740C>T	ENSP00000421655.2:p.Ala1247Val
ENST00000513346.5:c.3740C>T	ENSP00000427484.1:p.Ala1247Val
ENST00000514442.5:n.3790C>T
ENST00000515516.1:c.343-3232C>T	ENSP00000426471.1:n.343-3232C>T
NM_000356.3:c.3509C>T	NP_000347.2:p.Ala1170Val
NM_001135243.1:c.3740C>T	NP_001128715.1:p.Ala1247Val
NM_001135244.1:c.3629C>T	NP_001128716.1:p.Ala1210Val
NM_001135245.1:c.3512C>T	NP_001128717.1:p.Ala1171Val
NM_001195141.1:c.3626C>T	NP_001182070.1:p.Ala1209Val
XM_005268502.2:c.3854C>T	XP_005268559.1:p.Ala1285Val
XM_005268503.2:c.3851C>T	XP_005268560.1:p.Ala1284Val
XM_005268504.2:c.3851C>T	XP_005268561.1:p.Ala1284Val
XM_005268505.2:c.3743C>T	XP_005268562.1:p.Ala1248Val
XM_005268506.2:c.3740C>T	XP_005268563.1:p.Ala1247Val
XM_005268507.2:c.3623C>T	XP_005268564.1:p.Ala1208Val
XM_011537678.1:c.3674C>T	XP_011535980.1:p.Ala1225Val
XR_427778.1:n.3858C>T
XR_427780.1:n.3747C>T
XM_005268502.4:c.3854C>T	XP_005268559.1:p.Ala1285Val
XM_005268503.4:c.3851C>T	XP_005268560.1:p.Ala1284Val
XM_005268504.4:c.3851C>T	XP_005268561.1:p.Ala1284Val
XM_005268505.4:c.3743C>T	XP_005268562.1:p.Ala1248Val
XM_005268506.4:c.3740C>T	XP_005268563.1:p.Ala1247Val
XM_005268507.4:c.3623C>T	XP_005268564.1:p.Ala1208Val
XM_011537678.3:c.3674C>T	XP_011535980.1:p.Ala1225Val
XM_017009792.2:c.3737C>T	XP_016865281.1:p.Ala1246Val
XM_017009793.2:c.3563C>T	XP_016865282.1:p.Ala1188Val
XM_017009794.2:c.3449C>T	XP_016865283.1:p.Ala1150Val
XR_427778.3:n.3860C>T
XR_427780.3:n.3749C>T
NM_000356.4:c.3509C>T	NP_000347.2:p.Ala1170Val
NM_001135244.2:c.3629C>T	NP_001128716.1:p.Ala1210Val
NM_001135245.2:c.3512C>T	NP_001128717.1:p.Ala1171Val
NM_001195141.2:c.3626C>T	NP_001182070.1:p.Ala1209Val
NM_001371623.1:c.3743C>T MANE Select	NP_001358552.1:p.Ala1248Val
NM_001135243.2:c.3740C>T	NP_001128715.1:p.Ala1247Val