Canonical Allele Identifier: CA2639836496

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524587-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524587C>T , CM000679.2:g.75524587C>T	GRCh38
NC_000017.10:g.73520668C>T , CM000679.1:g.73520668C>T	GRCh37
NC_000017.9:g.71032263C>T	NCBI36
NG_013041.1:g.13060C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*175C>T MANE Select	ENSP00000327487.6:n.*175C>T
ENST00000434205.8:c.*175C>T	ENSP00000406559.4:n.*175C>T
ENST00000545228.3:c.*255C>T	ENSP00000438169.3:n.*255C>T
ENST00000577197.2:n.954C>T
ENST00000579449.2:n.2496C>T
ENST00000580013.6:n.2900C>T
ENST00000679370.1:n.3278C>T
ENST00000679429.1:c.*1214C>T	ENSP00000505403.1:n.*1214C>T
ENST00000679443.1:n.1825C>T
ENST00000679782.1:c.*455C>T	ENSP00000505995.1:n.*455C>T
ENST00000679919.1:n.2027C>T
ENST00000679928.1:c.*2308C>T	ENSP00000506071.1:n.*2308C>T
ENST00000680999.1:c.*175C>T	ENSP00000504984.1:n.*175C>T
ENST00000681282.1:c.*1943C>T	ENSP00000506339.1:n.*1943C>T
ENST00000333213.10:c.*175C>T	ENSP00000327487.6:n.*175C>T
ENST00000545228.2:c.1033C>T
ENST00000577197.1:n.504C>T
NM_207346.2:c.*175C>T	NP_997229.2:n.*175C>T
XM_005257229.2:c.*255C>T	XP_005257286.1:n.*255C>T
XM_006721821.2:c.*255C>T	XP_006721884.1:n.*255C>T
XM_011524616.1:c.*255C>T	XP_011522918.1:n.*255C>T
XM_011524618.1:c.*175C>T	XP_011522920.1:n.*175C>T
XR_243646.2:n.1988C>T
XM_005257229.4:c.*255C>T	XP_005257286.1:n.*255C>T
XR_243646.4:n.1994C>T
NM_207346.3:c.*175C>T MANE Select	NP_997229.2:n.*175C>T