Canonical Allele Identifier: CA2639836414

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75524557-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524557T>A , CM000679.2:g.75524557T>A	GRCh38
NC_000017.10:g.73520638T>A , CM000679.1:g.73520638T>A	GRCh37
NC_000017.9:g.71032233T>A	NCBI36
NG_013041.1:g.13030T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*145T>A MANE Select	ENSP00000327487.6:n.*145T>A
ENST00000434205.8:c.*145T>A	ENSP00000406559.4:n.*145T>A
ENST00000545228.3:c.*225T>A	ENSP00000438169.3:n.*225T>A
ENST00000577197.2:n.924T>A
ENST00000579449.2:n.2466T>A
ENST00000580013.6:n.2870T>A
ENST00000679370.1:n.3248T>A
ENST00000679429.1:c.*1184T>A	ENSP00000505403.1:n.*1184T>A
ENST00000679443.1:n.1795T>A
ENST00000679782.1:c.*425T>A	ENSP00000505995.1:n.*425T>A
ENST00000679919.1:n.1997T>A
ENST00000679928.1:c.*2278T>A	ENSP00000506071.1:n.*2278T>A
ENST00000680999.1:c.*145T>A	ENSP00000504984.1:n.*145T>A
ENST00000681282.1:c.*1913T>A	ENSP00000506339.1:n.*1913T>A
ENST00000333213.10:c.*145T>A	ENSP00000327487.6:n.*145T>A
ENST00000545228.2:c.1003T>A
ENST00000577197.1:n.474T>A
NM_207346.2:c.*145T>A	NP_997229.2:n.*145T>A
XM_005257229.2:c.*225T>A	XP_005257286.1:n.*225T>A
XM_006721821.2:c.*225T>A	XP_006721884.1:n.*225T>A
XM_011524616.1:c.*225T>A	XP_011522918.1:n.*225T>A
XM_011524618.1:c.*145T>A	XP_011522920.1:n.*145T>A
XR_243646.2:n.1958T>A
XM_005257229.4:c.*225T>A	XP_005257286.1:n.*225T>A
XR_243646.4:n.1964T>A
NM_207346.3:c.*145T>A MANE Select	NP_997229.2:n.*145T>A