Canonical Allele Identifier: CA447157949

Gene: TCOF1

Linked Data

• MyVariant Identifiers: chr5:g.149772997C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150393434C>A , CM000667.2:g.150393434C>A	GRCh38
NC_000005.9:g.149772997C>A , CM000667.1:g.149772997C>A	GRCh37
NC_000005.8:g.149753190C>A	NCBI36
NG_011341.1:g.40796C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.3549C>A	ENSP00000390717.3:p.Ala1183=
ENST00000643257.2:c.3666C>A MANE Select	ENSP00000493815.1:p.Ala1222=
ENST00000650162.1:c.3321C>A	ENSP00000497075.1:p.Ala1107=
ENST00000674413.1:c.3065C>A
ENST00000323668.11:c.3432C>A	ENSP00000325223.6:p.Ala1144=
ENST00000377797.7:c.3663C>A	ENSP00000367028.4:p.Ala1221=
ENST00000427724.6:c.3549C>A	ENSP00000390717.2:p.Ala1183=
ENST00000439160.6:c.3552C>A	ENSP00000406888.2:p.Ala1184=
ENST00000445265.6:c.3435C>A	ENSP00000409944.2:p.Ala1145=
ENST00000504761.6:c.3663C>A	ENSP00000421655.2:p.Ala1221=
ENST00000513346.5:c.3663C>A	ENSP00000427484.1:p.Ala1221=
ENST00000514442.5:n.3713C>A
ENST00000515516.1:c.343-3309C>A	ENSP00000426471.1:n.343-3309C>A
NM_000356.3:c.3432C>A	NP_000347.2:p.Ala1144=
NM_001135243.1:c.3663C>A	NP_001128715.1:p.Ala1221=
NM_001135244.1:c.3552C>A	NP_001128716.1:p.Ala1184=
NM_001135245.1:c.3435C>A	NP_001128717.1:p.Ala1145=
NM_001195141.1:c.3549C>A	NP_001182070.1:p.Ala1183=
XM_005268502.2:c.3777C>A	XP_005268559.1:p.Ala1259=
XM_005268503.2:c.3774C>A	XP_005268560.1:p.Ala1258=
XM_005268504.2:c.3774C>A	XP_005268561.1:p.Ala1258=
XM_005268505.2:c.3666C>A	XP_005268562.1:p.Ala1222=
XM_005268506.2:c.3663C>A	XP_005268563.1:p.Ala1221=
XM_005268507.2:c.3546C>A	XP_005268564.1:p.Ala1182=
XM_011537678.1:c.3597C>A	XP_011535980.1:p.Ala1199=
XR_427778.1:n.3781C>A
XR_427780.1:n.3670C>A
XM_005268502.4:c.3777C>A	XP_005268559.1:p.Ala1259=
XM_005268503.4:c.3774C>A	XP_005268560.1:p.Ala1258=
XM_005268504.4:c.3774C>A	XP_005268561.1:p.Ala1258=
XM_005268505.4:c.3666C>A	XP_005268562.1:p.Ala1222=
XM_005268506.4:c.3663C>A	XP_005268563.1:p.Ala1221=
XM_005268507.4:c.3546C>A	XP_005268564.1:p.Ala1182=
XM_011537678.3:c.3597C>A	XP_011535980.1:p.Ala1199=
XM_017009792.2:c.3660C>A	XP_016865281.1:p.Ala1220=
XM_017009793.2:c.3486C>A	XP_016865282.1:p.Ala1162=
XM_017009794.2:c.3372C>A	XP_016865283.1:p.Ala1124=
XR_427778.3:n.3783C>A
XR_427780.3:n.3672C>A
NM_000356.4:c.3432C>A	NP_000347.2:p.Ala1144=
NM_001135244.2:c.3552C>A	NP_001128716.1:p.Ala1184=
NM_001135245.2:c.3435C>A	NP_001128717.1:p.Ala1145=
NM_001195141.2:c.3549C>A	NP_001182070.1:p.Ala1183=
NM_001371623.1:c.3666C>A MANE Select	NP_001358552.1:p.Ala1222=
NM_001135243.2:c.3663C>A	NP_001128715.1:p.Ala1221=