Canonical Allele Identifier: CA1590925972

Gene: TCOF1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150393385G= , CM000667.2:g.150393385G=	GRCh38
NC_000005.9:g.149772948G= , CM000667.1:g.149772948G=	GRCh37
NC_000005.8:g.149753141G=	NCBI36
NG_011341.1:g.40747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.3500G=	ENSP00000390717.3:p.Gly1167=
ENST00000643257.2:c.3617G= MANE Select	ENSP00000493815.1:p.Gly1206=
ENST00000650162.1:c.3272G=	ENSP00000497075.1:p.Gly1091=
ENST00000674413.1:c.3016G=
ENST00000323668.11:c.3383G=	ENSP00000325223.6:p.Gly1128=
ENST00000377797.7:c.3614G=	ENSP00000367028.4:p.Gly1205=
ENST00000427724.6:c.3500G=	ENSP00000390717.2:p.Gly1167=
ENST00000439160.6:c.3503G=	ENSP00000406888.2:p.Gly1168=
ENST00000445265.6:c.3386G=	ENSP00000409944.2:p.Gly1129=
ENST00000504761.6:c.3614G=	ENSP00000421655.2:p.Gly1205=
ENST00000513346.5:c.3614G=	ENSP00000427484.1:p.Gly1205=
ENST00000514442.5:n.3664G=
ENST00000515516.1:c.343-3358G=	ENSP00000426471.1:n.343-3358G=
NM_000356.3:c.3383G=	NP_000347.2:p.Gly1128=
NM_001135243.1:c.3614G=	NP_001128715.1:p.Gly1205=
NM_001135244.1:c.3503G=	NP_001128716.1:p.Gly1168=
NM_001135245.1:c.3386G=	NP_001128717.1:p.Gly1129=
NM_001195141.1:c.3500G=	NP_001182070.1:p.Gly1167=
XM_005268502.2:c.3728G=	XP_005268559.1:p.Gly1243=
XM_005268503.2:c.3725G=	XP_005268560.1:p.Gly1242=
XM_005268504.2:c.3725G=	XP_005268561.1:p.Gly1242=
XM_005268505.2:c.3617G=	XP_005268562.1:p.Gly1206=
XM_005268506.2:c.3614G=	XP_005268563.1:p.Gly1205=
XM_005268507.2:c.3497G=	XP_005268564.1:p.Gly1166=
XM_011537678.1:c.3548G=	XP_011535980.1:p.Gly1183=
XR_427778.1:n.3732G=
XR_427780.1:n.3621G=
XM_005268502.4:c.3728G=	XP_005268559.1:p.Gly1243=
XM_005268503.4:c.3725G=	XP_005268560.1:p.Gly1242=
XM_005268504.4:c.3725G=	XP_005268561.1:p.Gly1242=
XM_005268505.4:c.3617G=	XP_005268562.1:p.Gly1206=
XM_005268506.4:c.3614G=	XP_005268563.1:p.Gly1205=
XM_005268507.4:c.3497G=	XP_005268564.1:p.Gly1166=
XM_011537678.3:c.3548G=	XP_011535980.1:p.Gly1183=
XM_017009792.2:c.3611G=	XP_016865281.1:p.Gly1204=
XM_017009793.2:c.3437G=	XP_016865282.1:p.Gly1146=
XM_017009794.2:c.3323G=	XP_016865283.1:p.Gly1108=
XR_427778.3:n.3734G=
XR_427780.3:n.3623G=
NM_000356.4:c.3383G=	NP_000347.2:p.Gly1128=
NM_001135244.2:c.3503G=	NP_001128716.1:p.Gly1168=
NM_001135245.2:c.3386G=	NP_001128717.1:p.Gly1129=
NM_001195141.2:c.3500G=	NP_001182070.1:p.Gly1167=
NM_001371623.1:c.3617G= MANE Select	NP_001358552.1:p.Gly1206=
NM_001135243.2:c.3614G=	NP_001128715.1:p.Gly1205=