Canonical Allele Identifier: CA2639835453

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75523914-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75523914C>A , CM000679.2:g.75523914C>A	GRCh38
NC_000017.10:g.73519995C>A , CM000679.1:g.73519995C>A	GRCh37
NC_000017.9:g.71031590C>A	NCBI36
NG_013041.1:g.12387C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1430+135C>A MANE Select	ENSP00000327487.6:n.1430+135C>A
ENST00000434205.8:c.1127+135C>A	ENSP00000406559.4:n.1127+135C>A
ENST00000545228.3:c.1618+135C>A	ENSP00000438169.3:n.1618+135C>A
ENST00000577197.2:n.628+135C>A
ENST00000579449.2:n.2170+135C>A
ENST00000580013.6:n.2574+135C>A
ENST00000679370.1:n.2952+135C>A
ENST00000679429.1:c.*888+135C>A	ENSP00000505403.1:n.*888+135C>A
ENST00000679443.1:n.1499+135C>A
ENST00000679782.1:c.*129+135C>A	ENSP00000505995.1:n.*129+135C>A
ENST00000679919.1:n.1701+135C>A
ENST00000679928.1:c.*1982+135C>A	ENSP00000506071.1:n.*1982+135C>A
ENST00000680528.1:n.2396+135C>A
ENST00000680999.1:c.1643+135C>A	ENSP00000504984.1:n.1643+135C>A
ENST00000681282.1:c.*1617+135C>A	ENSP00000506339.1:n.*1617+135C>A
ENST00000333213.10:c.1430+135C>A	ENSP00000327487.6:n.1430+135C>A
ENST00000545228.2:c.707+135C>A
ENST00000577197.1:n.178+135C>A
ENST00000579449.1:n.627+135C>A
NM_207346.2:c.1430+135C>A	NP_997229.2:n.1430+135C>A
XM_005257229.2:c.1618+135C>A	XP_005257286.1:n.1618+135C>A
XM_006721821.2:c.1315+135C>A	XP_006721884.1:n.1315+135C>A
XM_011524616.1:c.1502-348C>A	XP_011522918.1:n.1502-348C>A
XM_011524617.1:c.*13-348C>A	XP_011522919.1:n.*13-348C>A
XM_011524618.1:c.1314-348C>A	XP_011522920.1:n.1314-348C>A
XR_243646.2:n.1662+135C>A
XM_005257229.4:c.1618+135C>A	XP_005257286.1:n.1618+135C>A
XR_001753015.1:n.87+397G>T
XR_001753016.1:n.88+397G>T
XR_243646.4:n.1668+135C>A
NM_207346.3:c.1430+135C>A MANE Select	NP_997229.2:n.1430+135C>A