Canonical Allele Identifier: CA2639836237

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524462-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524462C>A , CM000679.2:g.75524462C>A	GRCh38
NC_000017.10:g.73520543C>A , CM000679.1:g.73520543C>A	GRCh37
NC_000017.9:g.71032138C>A	NCBI36
NG_013041.1:g.12935C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*50C>A MANE Select	ENSP00000327487.6:n.*50C>A
ENST00000434205.8:c.*50C>A	ENSP00000406559.4:n.*50C>A
ENST00000545228.3:c.*130C>A	ENSP00000438169.3:n.*130C>A
ENST00000577197.2:n.829C>A
ENST00000579449.2:n.2371C>A
ENST00000580013.6:n.2775C>A
ENST00000679370.1:n.3153C>A
ENST00000679429.1:c.*1089C>A	ENSP00000505403.1:n.*1089C>A
ENST00000679443.1:n.1700C>A
ENST00000679782.1:c.*330C>A	ENSP00000505995.1:n.*330C>A
ENST00000679919.1:n.1902C>A
ENST00000679928.1:c.*2183C>A	ENSP00000506071.1:n.*2183C>A
ENST00000680999.1:c.*50C>A	ENSP00000504984.1:n.*50C>A
ENST00000681282.1:c.*1818C>A	ENSP00000506339.1:n.*1818C>A
ENST00000333213.10:c.*50C>A	ENSP00000327487.6:n.*50C>A
ENST00000545228.2:c.908C>A
ENST00000577197.1:n.379C>A
NM_207346.2:c.*50C>A	NP_997229.2:n.*50C>A
XM_005257229.2:c.*130C>A	XP_005257286.1:n.*130C>A
XM_006721821.2:c.*130C>A	XP_006721884.1:n.*130C>A
XM_011524616.1:c.*130C>A	XP_011522918.1:n.*130C>A
XM_011524618.1:c.*50C>A	XP_011522920.1:n.*50C>A
XR_243646.2:n.1863C>A
XM_005257229.4:c.*130C>A	XP_005257286.1:n.*130C>A
XR_243646.4:n.1869C>A
NM_207346.3:c.*50C>A MANE Select	NP_997229.2:n.*50C>A