Canonical Allele Identifier: CA2639836340

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524520-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524520G>A , CM000679.2:g.75524520G>A	GRCh38
NC_000017.10:g.73520601G>A , CM000679.1:g.73520601G>A	GRCh37
NC_000017.9:g.71032196G>A	NCBI36
NG_013041.1:g.12993G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*108G>A MANE Select	ENSP00000327487.6:n.*108G>A
ENST00000434205.8:c.*108G>A	ENSP00000406559.4:n.*108G>A
ENST00000545228.3:c.*188G>A	ENSP00000438169.3:n.*188G>A
ENST00000577197.2:n.887G>A
ENST00000579449.2:n.2429G>A
ENST00000580013.6:n.2833G>A
ENST00000679370.1:n.3211G>A
ENST00000679429.1:c.*1147G>A	ENSP00000505403.1:n.*1147G>A
ENST00000679443.1:n.1758G>A
ENST00000679782.1:c.*388G>A	ENSP00000505995.1:n.*388G>A
ENST00000679919.1:n.1960G>A
ENST00000679928.1:c.*2241G>A	ENSP00000506071.1:n.*2241G>A
ENST00000680999.1:c.*108G>A	ENSP00000504984.1:n.*108G>A
ENST00000681282.1:c.*1876G>A	ENSP00000506339.1:n.*1876G>A
ENST00000333213.10:c.*108G>A	ENSP00000327487.6:n.*108G>A
ENST00000545228.2:c.966G>A
ENST00000577197.1:n.437G>A
NM_207346.2:c.*108G>A	NP_997229.2:n.*108G>A
XM_005257229.2:c.*188G>A	XP_005257286.1:n.*188G>A
XM_006721821.2:c.*188G>A	XP_006721884.1:n.*188G>A
XM_011524616.1:c.*188G>A	XP_011522918.1:n.*188G>A
XM_011524618.1:c.*108G>A	XP_011522920.1:n.*108G>A
XR_243646.2:n.1921G>A
XM_005257229.4:c.*188G>A	XP_005257286.1:n.*188G>A
XR_243646.4:n.1927G>A
NM_207346.3:c.*108G>A MANE Select	NP_997229.2:n.*108G>A