Canonical Allele Identifier: CA361759120

Gene: TCOF1

Linked Data

• MyVariant Identifiers: chr5:g.149759128G>A (hg19) ; chr5:g.150379565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150379565G>A , CM000667.2:g.150379565G>A	GRCh38
NC_000005.9:g.149759128G>A , CM000667.1:g.149759128G>A	GRCh37
NC_000005.8:g.149739321G>A	NCBI36
NG_011341.1:g.26927G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427724.7:c.2692G>A	ENSP00000390717.3:p.Ala898Thr
ENST00000513538.2:c.2692G>A	ENSP00000422567.2:p.Ala898Thr
ENST00000643257.2:c.2692G>A MANE Select	ENSP00000493815.1:p.Ala898Thr
ENST00000650162.1:c.2461G>A	ENSP00000497075.1:p.Ala821Thr
ENST00000674413.1:c.1980G>A
ENST00000323668.11:c.2461G>A	ENSP00000325223.6:p.Ala821Thr
ENST00000377797.7:c.2692G>A	ENSP00000367028.4:p.Ala898Thr
ENST00000394269.7:c.2692G>A	ENSP00000377811.3:p.Ala898Thr
ENST00000427724.6:c.2692G>A	ENSP00000390717.2:p.Ala898Thr
ENST00000439160.6:c.2692G>A	ENSP00000406888.2:p.Ala898Thr
ENST00000445265.6:c.2461G>A	ENSP00000409944.2:p.Ala821Thr
ENST00000504761.6:c.2692G>A	ENSP00000421655.2:p.Ala898Thr
ENST00000506063.1:n.447G>A
ENST00000506767.1:c.167G>A
ENST00000513346.5:c.2692G>A	ENSP00000427484.1:p.Ala898Thr
ENST00000514442.5:n.1492G>A
ENST00000515035.5:n.3946G>A
ENST00000515516.1:c.342+11648G>A	ENSP00000426471.1:n.342+11648G>A
NM_000356.3:c.2461G>A	NP_000347.2:p.Ala821Thr
NM_001008657.2:c.2692G>A	NP_001008657.1:p.Ala898Thr
NM_001135243.1:c.2692G>A	NP_001128715.1:p.Ala898Thr
NM_001135244.1:c.2692G>A	NP_001128716.1:p.Ala898Thr
NM_001135245.1:c.2461G>A	NP_001128717.1:p.Ala821Thr
NM_001195141.1:c.2692G>A	NP_001182070.1:p.Ala898Thr
XM_005268502.2:c.2692G>A	XP_005268559.1:p.Ala898Thr
XM_005268503.2:c.2692G>A	XP_005268560.1:p.Ala898Thr
XM_005268504.2:c.2692G>A	XP_005268561.1:p.Ala898Thr
XM_005268505.2:c.2692G>A	XP_005268562.1:p.Ala898Thr
XM_005268506.2:c.2692G>A	XP_005268563.1:p.Ala898Thr
XM_005268507.2:c.2461G>A	XP_005268564.1:p.Ala821Thr
XM_005268508.2:c.2692G>A	XP_005268565.1:p.Ala898Thr
XM_005268509.2:c.2692G>A	XP_005268566.1:p.Ala898Thr
XM_011537678.1:c.2512G>A	XP_011535980.1:p.Ala838Thr
XR_427778.1:n.2737G>A
XR_427779.1:n.2737G>A
XR_427780.1:n.2737G>A
XM_005268502.4:c.2692G>A	XP_005268559.1:p.Ala898Thr
XM_005268503.4:c.2692G>A	XP_005268560.1:p.Ala898Thr
XM_005268504.4:c.2692G>A	XP_005268561.1:p.Ala898Thr
XM_005268505.4:c.2692G>A	XP_005268562.1:p.Ala898Thr
XM_005268506.4:c.2692G>A	XP_005268563.1:p.Ala898Thr
XM_005268507.4:c.2461G>A	XP_005268564.1:p.Ala821Thr
XM_005268508.4:c.2692G>A	XP_005268565.1:p.Ala898Thr
XM_005268509.4:c.2692G>A	XP_005268566.1:p.Ala898Thr
XM_011537678.3:c.2512G>A	XP_011535980.1:p.Ala838Thr
XM_017009792.2:c.2692G>A	XP_016865281.1:p.Ala898Thr
XM_017009793.2:c.2512G>A	XP_016865282.1:p.Ala838Thr
XM_017009794.2:c.2512G>A	XP_016865283.1:p.Ala838Thr
XM_017009795.2:c.2461G>A	XP_016865284.1:p.Ala821Thr
XR_427778.3:n.2739G>A
XR_427779.2:n.2739G>A
XR_427780.3:n.2739G>A
NM_000356.4:c.2461G>A	NP_000347.2:p.Ala821Thr
NM_001008657.3:c.2692G>A	NP_001008657.1:p.Ala898Thr
NM_001135244.2:c.2692G>A	NP_001128716.1:p.Ala898Thr
NM_001135245.2:c.2461G>A	NP_001128717.1:p.Ala821Thr
NM_001195141.2:c.2692G>A	NP_001182070.1:p.Ala898Thr
NM_001371623.1:c.2692G>A MANE Select	NP_001358552.1:p.Ala898Thr
NM_001135243.2:c.2692G>A	NP_001128715.1:p.Ala898Thr