Canonical Allele Identifier: CA401028164

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517495T>C (hg19) ; chr17:g.75521414T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521414T>C , CM000679.2:g.75521414T>C	GRCh38
NC_000017.10:g.73517495T>C , CM000679.1:g.73517495T>C	GRCh37
NC_000017.9:g.71029090T>C	NCBI36
NG_013041.1:g.9887T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.527T>C MANE Select	ENSP00000327487.6:p.Val176Ala
ENST00000434205.8:c.224T>C	ENSP00000406559.4:p.Val75Ala
ENST00000545228.3:c.527T>C	ENSP00000438169.3:p.Val176Ala
ENST00000579449.2:n.326T>C
ENST00000580013.6:n.536T>C
ENST00000583818.2:c.581T>C	ENSP00000461928.2:n.581T>C
ENST00000679370.1:n.914T>C
ENST00000679429.1:c.519T>C	ENSP00000505403.1:p.Cys173=
ENST00000679443.1:n.402T>C
ENST00000679782.1:c.527T>C	ENSP00000505995.1:p.Val176Ala
ENST00000679919.1:n.402T>C
ENST00000679928.1:c.*138T>C	ENSP00000506071.1:n.*138T>C
ENST00000680528.1:n.552T>C
ENST00000680999.1:c.527T>C	ENSP00000504984.1:p.Val176Ala
ENST00000681282.1:c.527T>C	ENSP00000506339.1:p.Val176Ala
ENST00000333213.10:c.527T>C	ENSP00000327487.6:p.Val176Ala
ENST00000578415.1:c.487T>C
ENST00000580013.5:n.544T>C
ENST00000583173.5:c.362T>C	ENSP00000463619.1:p.Val121Ala
ENST00000583818.1:c.476T>C	ENSP00000461928.1:n.476T>C
NM_207346.2:c.527T>C	NP_997229.2:p.Val176Ala
XM_005257229.2:c.527T>C	XP_005257286.1:p.Val176Ala
XM_006721821.2:c.224T>C	XP_006721884.1:p.Val75Ala
XM_011524616.1:c.527T>C	XP_011522918.1:p.Val176Ala
XM_011524617.1:c.527T>C	XP_011522919.1:p.Val176Ala
XM_011524618.1:c.527T>C	XP_011522920.1:p.Val176Ala
XR_243646.2:n.557T>C
XM_005257229.4:c.527T>C	XP_005257286.1:p.Val176Ala
XR_243646.4:n.563T>C
NM_207346.3:c.527T>C MANE Select	NP_997229.2:p.Val176Ala