Canonical Allele Identifier: CA2739561920

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524538G>C , CM000679.2:g.75524538G>C	GRCh38
NC_000017.10:g.73520619G>C , CM000679.1:g.73520619G>C	GRCh37
NC_000017.9:g.71032214G>C	NCBI36
NG_013041.1:g.13011G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*126G>C MANE Select	ENSP00000327487.6:n.*126G>C
ENST00000434205.8:c.*126G>C	ENSP00000406559.4:n.*126G>C
ENST00000545228.3:c.*206G>C	ENSP00000438169.3:n.*206G>C
ENST00000577197.2:n.905G>C
ENST00000579449.2:n.2447G>C
ENST00000580013.6:n.2851G>C
ENST00000679370.1:n.3229G>C
ENST00000679429.1:c.*1165G>C	ENSP00000505403.1:n.*1165G>C
ENST00000679443.1:n.1776G>C
ENST00000679782.1:c.*406G>C	ENSP00000505995.1:n.*406G>C
ENST00000679919.1:n.1978G>C
ENST00000679928.1:c.*2259G>C	ENSP00000506071.1:n.*2259G>C
ENST00000680999.1:c.*126G>C	ENSP00000504984.1:n.*126G>C
ENST00000681282.1:c.*1894G>C	ENSP00000506339.1:n.*1894G>C
ENST00000333213.10:c.*126G>C	ENSP00000327487.6:n.*126G>C
ENST00000545228.2:c.984G>C
ENST00000577197.1:n.455G>C
NM_207346.2:c.*126G>C	NP_997229.2:n.*126G>C
XM_005257229.2:c.*206G>C	XP_005257286.1:n.*206G>C
XM_006721821.2:c.*206G>C	XP_006721884.1:n.*206G>C
XM_011524616.1:c.*206G>C	XP_011522918.1:n.*206G>C
XM_011524618.1:c.*126G>C	XP_011522920.1:n.*126G>C
XR_243646.2:n.1939G>C
XM_005257229.4:c.*206G>C	XP_005257286.1:n.*206G>C
XR_243646.4:n.1945G>C
NM_207346.3:c.*126G>C MANE Select	NP_997229.2:n.*126G>C