Canonical Allele Identifier: CA2639822779

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75516976-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516976G>T , CM000679.2:g.75516976G>T	GRCh38
NC_000017.10:g.73513057G>T , CM000679.1:g.73513057G>T	GRCh37
NC_000017.9:g.71024652G>T	NCBI36
NG_013041.1:g.5449G>T
NG_033152.1:g.3608C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.222-33G>T MANE Select	ENSP00000327487.6:n.222-33G>T
ENST00000434205.8:c.-82-33G>T	ENSP00000406559.4:n.-82-33G>T
ENST00000545228.3:c.222-33G>T	ENSP00000438169.3:n.222-33G>T
ENST00000579449.2:n.21-33G>T
ENST00000580013.6:n.231-33G>T
ENST00000583818.2:c.222-33G>T	ENSP00000461928.2:n.222-33G>T
ENST00000679370.1:n.609-33G>T
ENST00000679429.1:c.222-33G>T	ENSP00000505403.1:n.222-33G>T
ENST00000679443.1:n.97-33G>T
ENST00000679782.1:c.222-33G>T	ENSP00000505995.1:n.222-33G>T
ENST00000679919.1:n.97-33G>T
ENST00000679928.1:c.222-33G>T	ENSP00000506071.1:n.222-33G>T
ENST00000680528.1:n.247-33G>T
ENST00000680999.1:c.222-33G>T	ENSP00000504984.1:n.222-33G>T
ENST00000681282.1:c.222-33G>T	ENSP00000506339.1:n.222-33G>T
ENST00000333213.10:c.222-33G>T	ENSP00000327487.6:n.222-33G>T
ENST00000434205.7:c.-82-33G>T	ENSP00000406559.3:n.-82-33G>T
ENST00000578415.1:c.100-39G>T
ENST00000580013.5:n.247-33G>T
ENST00000583173.5:c.57-33G>T	ENSP00000463619.1:n.57-33G>T
ENST00000583454.1:n.322G>T
ENST00000583634.1:n.7G>T
ENST00000583818.1:c.117-33G>T	ENSP00000461928.1:n.117-33G>T
NM_207346.2:c.222-33G>T	NP_997229.2:n.222-33G>T
XM_005257229.2:c.222-33G>T	XP_005257286.1:n.222-33G>T
XM_006721821.2:c.-82-33G>T	XP_006721884.1:n.-82-33G>T
XM_011524616.1:c.222-33G>T	XP_011522918.1:n.222-33G>T
XM_011524617.1:c.222-33G>T	XP_011522919.1:n.222-33G>T
XM_011524618.1:c.222-33G>T	XP_011522920.1:n.222-33G>T
XR_243646.2:n.252-33G>T
XM_005257229.4:c.222-33G>T	XP_005257286.1:n.222-33G>T
XR_243646.4:n.258-33G>T
NM_207346.3:c.222-33G>T MANE Select	NP_997229.2:n.222-33G>T