Canonical Allele Identifier: CA2639836265

Gene: TSEN54

Linked Data

• ClinVar Variation Id: 2701616
• ClinVar RCV Id: RCV003549768
• gnomAD v4: 17-75516740-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516740C>T , CM000679.2:g.75516740C>T	GRCh38
NC_000017.10:g.73512821C>T , CM000679.1:g.73512821C>T	GRCh37
NC_000017.9:g.71024416C>T	NCBI36
NG_013041.1:g.5213C>T
NG_033152.1:g.3844G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.57-6C>T MANE Select	ENSP00000327487.6:n.57-6C>T
ENST00000434205.8:c.-82-269C>T	ENSP00000406559.4:n.-82-269C>T
ENST00000545228.3:c.57-6C>T	ENSP00000438169.3:n.57-6C>T
ENST00000579449.2:n.20+124C>T
ENST00000580013.6:n.66-6C>T
ENST00000583818.2:c.57-6C>T	ENSP00000461928.2:n.57-6C>T
ENST00000679370.1:n.444-6C>T
ENST00000679429.1:c.57-6C>T	ENSP00000505403.1:n.57-6C>T
ENST00000679782.1:c.57-6C>T	ENSP00000505995.1:n.57-6C>T
ENST00000679928.1:c.57-6C>T	ENSP00000506071.1:n.57-6C>T
ENST00000680528.1:n.82-6C>T
ENST00000680999.1:c.57-6C>T	ENSP00000504984.1:n.57-6C>T
ENST00000681282.1:c.57-6C>T	ENSP00000506339.1:n.57-6C>T
ENST00000333213.10:c.57-6C>T	ENSP00000327487.6:n.57-6C>T
ENST00000434205.7:c.-82-269C>T	ENSP00000406559.3:n.-82-269C>T
ENST00000580013.5:n.82-6C>T
ENST00000583173.5:c.56+124C>T	ENSP00000463619.1:n.56+124C>T
ENST00000583454.1:n.92-6C>T
NM_207346.2:c.57-6C>T	NP_997229.2:n.57-6C>T
XM_005257229.2:c.57-6C>T	XP_005257286.1:n.57-6C>T
XM_006721821.2:c.-247-6C>T	XP_006721884.1:n.-247-6C>T
XM_011524616.1:c.57-6C>T	XP_011522918.1:n.57-6C>T
XM_011524617.1:c.57-6C>T	XP_011522919.1:n.57-6C>T
XM_011524618.1:c.57-6C>T	XP_011522920.1:n.57-6C>T
XR_243646.2:n.87-6C>T
XM_005257229.4:c.57-6C>T	XP_005257286.1:n.57-6C>T
XR_243646.4:n.93-6C>T
NM_207346.3:c.57-6C>T MANE Select	NP_997229.2:n.57-6C>T