Canonical Allele Identifier: CA401029001

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517946G>C (hg19) ; chr17:g.75521865G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521865G>C , CM000679.2:g.75521865G>C	GRCh38
NC_000017.10:g.73517946G>C , CM000679.1:g.73517946G>C	GRCh37
NC_000017.9:g.71029541G>C	NCBI36
NG_013041.1:g.10338G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.784G>C MANE Select	ENSP00000327487.6:p.Gly262Arg
ENST00000434205.8:c.481G>C	ENSP00000406559.4:p.Gly161Arg
ENST00000545228.3:c.784G>C	ENSP00000438169.3:p.Gly262Arg
ENST00000579449.2:n.583G>C
ENST00000580013.6:n.987G>C
ENST00000583818.2:c.838G>C	ENSP00000461928.2:n.838G>C
ENST00000679370.1:n.1365G>C
ENST00000679429.1:c.*242G>C	ENSP00000505403.1:n.*242G>C
ENST00000679443.1:n.853G>C
ENST00000679782.1:c.784G>C	ENSP00000505995.1:p.Gly262Arg
ENST00000679919.1:n.853G>C
ENST00000679928.1:c.*395G>C	ENSP00000506071.1:n.*395G>C
ENST00000680528.1:n.809G>C
ENST00000680999.1:c.784G>C	ENSP00000504984.1:p.Gly262Arg
ENST00000681282.1:c.*30G>C	ENSP00000506339.1:n.*30G>C
ENST00000333213.10:c.784G>C	ENSP00000327487.6:p.Gly262Arg
ENST00000578415.1:c.744G>C
ENST00000583173.5:c.459-142G>C	ENSP00000463619.1:n.459-142G>C
ENST00000583818.1:c.733G>C	ENSP00000461928.1:n.733G>C
NM_207346.2:c.784G>C	NP_997229.2:p.Gly262Arg
XM_005257229.2:c.784G>C	XP_005257286.1:p.Gly262Arg
XM_006721821.2:c.481G>C	XP_006721884.1:p.Gly161Arg
XM_011524616.1:c.784G>C	XP_011522918.1:p.Gly262Arg
XM_011524617.1:c.784G>C	XP_011522919.1:p.Gly262Arg
XM_011524618.1:c.784G>C	XP_011522920.1:p.Gly262Arg
XR_243646.2:n.814G>C
XM_005257229.4:c.784G>C	XP_005257286.1:p.Gly262Arg
XR_243646.4:n.820G>C
NM_207346.3:c.784G>C MANE Select	NP_997229.2:p.Gly262Arg