Canonical Allele Identifier: CA2739561928

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524546G>A , CM000679.2:g.75524546G>A	GRCh38
NC_000017.10:g.73520627G>A , CM000679.1:g.73520627G>A	GRCh37
NC_000017.9:g.71032222G>A	NCBI36
NG_013041.1:g.13019G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*134G>A MANE Select	ENSP00000327487.6:n.*134G>A
ENST00000434205.8:c.*134G>A	ENSP00000406559.4:n.*134G>A
ENST00000545228.3:c.*214G>A	ENSP00000438169.3:n.*214G>A
ENST00000577197.2:n.913G>A
ENST00000579449.2:n.2455G>A
ENST00000580013.6:n.2859G>A
ENST00000679370.1:n.3237G>A
ENST00000679429.1:c.*1173G>A	ENSP00000505403.1:n.*1173G>A
ENST00000679443.1:n.1784G>A
ENST00000679782.1:c.*414G>A	ENSP00000505995.1:n.*414G>A
ENST00000679919.1:n.1986G>A
ENST00000679928.1:c.*2267G>A	ENSP00000506071.1:n.*2267G>A
ENST00000680999.1:c.*134G>A	ENSP00000504984.1:n.*134G>A
ENST00000681282.1:c.*1902G>A	ENSP00000506339.1:n.*1902G>A
ENST00000333213.10:c.*134G>A	ENSP00000327487.6:n.*134G>A
ENST00000545228.2:c.992G>A
ENST00000577197.1:n.463G>A
NM_207346.2:c.*134G>A	NP_997229.2:n.*134G>A
XM_005257229.2:c.*214G>A	XP_005257286.1:n.*214G>A
XM_006721821.2:c.*214G>A	XP_006721884.1:n.*214G>A
XM_011524616.1:c.*214G>A	XP_011522918.1:n.*214G>A
XM_011524618.1:c.*134G>A	XP_011522920.1:n.*134G>A
XR_243646.2:n.1947G>A
XM_005257229.4:c.*214G>A	XP_005257286.1:n.*214G>A
XR_243646.4:n.1953G>A
NM_207346.3:c.*134G>A MANE Select	NP_997229.2:n.*134G>A