Canonical Allele Identifier: CA401029038

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517958C>A (hg19) ; chr17:g.75521877C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521877C>A , CM000679.2:g.75521877C>A	GRCh38
NC_000017.10:g.73517958C>A , CM000679.1:g.73517958C>A	GRCh37
NC_000017.9:g.71029553C>A	NCBI36
NG_013041.1:g.10350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.796C>A MANE Select	ENSP00000327487.6:p.Pro266Thr
ENST00000434205.8:c.493C>A	ENSP00000406559.4:p.Pro165Thr
ENST00000545228.3:c.796C>A	ENSP00000438169.3:p.Pro266Thr
ENST00000579449.2:n.595C>A
ENST00000580013.6:n.999C>A
ENST00000583818.2:c.850C>A	ENSP00000461928.2:n.850C>A
ENST00000679370.1:n.1377C>A
ENST00000679429.1:c.*254C>A	ENSP00000505403.1:n.*254C>A
ENST00000679443.1:n.865C>A
ENST00000679782.1:c.796C>A	ENSP00000505995.1:p.Pro266Thr
ENST00000679919.1:n.865C>A
ENST00000679928.1:c.*407C>A	ENSP00000506071.1:n.*407C>A
ENST00000680528.1:n.821C>A
ENST00000680999.1:c.796C>A	ENSP00000504984.1:p.Pro266Thr
ENST00000681282.1:c.*42C>A	ENSP00000506339.1:n.*42C>A
ENST00000333213.10:c.796C>A	ENSP00000327487.6:p.Pro266Thr
ENST00000578415.1:c.756C>A
ENST00000583173.5:c.459-130C>A	ENSP00000463619.1:n.459-130C>A
ENST00000583818.1:c.745C>A	ENSP00000461928.1:n.745C>A
NM_207346.2:c.796C>A	NP_997229.2:p.Pro266Thr
XM_005257229.2:c.796C>A	XP_005257286.1:p.Pro266Thr
XM_006721821.2:c.493C>A	XP_006721884.1:p.Pro165Thr
XM_011524616.1:c.796C>A	XP_011522918.1:p.Pro266Thr
XM_011524617.1:c.796C>A	XP_011522919.1:p.Pro266Thr
XM_011524618.1:c.796C>A	XP_011522920.1:p.Pro266Thr
XR_243646.2:n.826C>A
XM_005257229.4:c.796C>A	XP_005257286.1:p.Pro266Thr
XR_243646.4:n.832C>A
NM_207346.3:c.796C>A MANE Select	NP_997229.2:p.Pro266Thr