Canonical Allele Identifier: CA2639836516

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524596-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524596C>A , CM000679.2:g.75524596C>A	GRCh38
NC_000017.10:g.73520677C>A , CM000679.1:g.73520677C>A	GRCh37
NC_000017.9:g.71032272C>A	NCBI36
NG_013041.1:g.13069C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*184C>A MANE Select	ENSP00000327487.6:n.*184C>A
ENST00000434205.8:c.*184C>A	ENSP00000406559.4:n.*184C>A
ENST00000545228.3:c.*264C>A	ENSP00000438169.3:n.*264C>A
ENST00000577197.2:n.963C>A
ENST00000579449.2:n.2505C>A
ENST00000580013.6:n.2909C>A
ENST00000679370.1:n.3287C>A
ENST00000679429.1:c.*1223C>A	ENSP00000505403.1:n.*1223C>A
ENST00000679443.1:n.1834C>A
ENST00000679782.1:c.*464C>A	ENSP00000505995.1:n.*464C>A
ENST00000679919.1:n.2036C>A
ENST00000679928.1:c.*2317C>A	ENSP00000506071.1:n.*2317C>A
ENST00000680999.1:c.*184C>A	ENSP00000504984.1:n.*184C>A
ENST00000681282.1:c.*1952C>A	ENSP00000506339.1:n.*1952C>A
ENST00000333213.10:c.*184C>A	ENSP00000327487.6:n.*184C>A
ENST00000545228.2:c.1042C>A
ENST00000577197.1:n.513C>A
NM_207346.2:c.*184C>A	NP_997229.2:n.*184C>A
XM_005257229.2:c.*264C>A	XP_005257286.1:n.*264C>A
XM_006721821.2:c.*264C>A	XP_006721884.1:n.*264C>A
XM_011524616.1:c.*264C>A	XP_011522918.1:n.*264C>A
XM_011524618.1:c.*184C>A	XP_011522920.1:n.*184C>A
XR_243646.2:n.1997C>A
XM_005257229.4:c.*264C>A	XP_005257286.1:n.*264C>A
XR_243646.4:n.2003C>A
NM_207346.3:c.*184C>A MANE Select	NP_997229.2:n.*184C>A