Canonical Allele Identifier: CA502045669

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517512A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521431A>C , CM000679.2:g.75521431A>C	GRCh38
NC_000017.10:g.73517512A>C , CM000679.1:g.73517512A>C	GRCh37
NC_000017.9:g.71029107A>C	NCBI36
NG_013041.1:g.9904A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.544A>C MANE Select	ENSP00000327487.6:p.Arg182=
ENST00000434205.8:c.241A>C	ENSP00000406559.4:p.Arg81=
ENST00000545228.3:c.544A>C	ENSP00000438169.3:p.Arg182=
ENST00000579449.2:n.343A>C
ENST00000580013.6:n.553A>C
ENST00000583818.2:c.598A>C	ENSP00000461928.2:n.598A>C
ENST00000679370.1:n.931A>C
ENST00000679429.1:c.*2A>C	ENSP00000505403.1:n.*2A>C
ENST00000679443.1:n.419A>C
ENST00000679782.1:c.544A>C	ENSP00000505995.1:p.Arg182=
ENST00000679919.1:n.419A>C
ENST00000679928.1:c.*155A>C	ENSP00000506071.1:n.*155A>C
ENST00000680528.1:n.569A>C
ENST00000680999.1:c.544A>C	ENSP00000504984.1:p.Arg182=
ENST00000681282.1:c.544A>C	ENSP00000506339.1:p.Arg182=
ENST00000333213.10:c.544A>C	ENSP00000327487.6:p.Arg182=
ENST00000578415.1:c.504A>C
ENST00000580013.5:n.561A>C
ENST00000583173.5:c.379A>C	ENSP00000463619.1:p.Arg127=
ENST00000583818.1:c.493A>C	ENSP00000461928.1:n.493A>C
NM_207346.2:c.544A>C	NP_997229.2:p.Arg182=
XM_005257229.2:c.544A>C	XP_005257286.1:p.Arg182=
XM_006721821.2:c.241A>C	XP_006721884.1:p.Arg81=
XM_011524616.1:c.544A>C	XP_011522918.1:p.Arg182=
XM_011524617.1:c.544A>C	XP_011522919.1:p.Arg182=
XM_011524618.1:c.544A>C	XP_011522920.1:p.Arg182=
XR_243646.2:n.574A>C
XM_005257229.4:c.544A>C	XP_005257286.1:p.Arg182=
XR_243646.4:n.580A>C
NM_207346.3:c.544A>C MANE Select	NP_997229.2:p.Arg182=