Canonical Allele Identifier: CA2275549733
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75519057C= , CM000679.2:g.75519057C= GRCh38
NC_000017.10:g.73515138C= , CM000679.1:g.73515138C= GRCh37
NC_000017.9:g.71026733C= NCBI36
NG_013041.1:g.7530C=
NG_033152.1:g.1527G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.521+10C= MANE Select ENSP00000327487.6:n.521+10C=
ENST00000434205.8:c.218+10C= ENSP00000406559.4:n.218+10C=
ENST00000545228.3:c.521+10C= ENSP00000438169.3:n.521+10C=
ENST00000579449.2:n.320+10C=
ENST00000580013.6:n.530+10C=
ENST00000583818.2:c.521+10C= ENSP00000461928.2:n.521+10C=
ENST00000679370.1:n.908+10C=
ENST00000679429.1:c.513+10C= ENSP00000505403.1:n.513+10C=
ENST00000679443.1:n.396+10C=
ENST00000679782.1:c.521+10C= ENSP00000505995.1:n.521+10C=
ENST00000679919.1:n.396+10C=
ENST00000679928.1:c.521+10C= ENSP00000506071.1:n.521+10C=
ENST00000680528.1:n.546+10C=
ENST00000680999.1:c.521+10C= ENSP00000504984.1:n.521+10C=
ENST00000681282.1:c.521+10C= ENSP00000506339.1:n.521+10C=
ENST00000333213.10:c.521+10C= ENSP00000327487.6:n.521+10C=
ENST00000578415.1:c.481+10C=
ENST00000580013.5:n.538+10C=
ENST00000583173.5:c.356+10C= ENSP00000463619.1:n.356+10C=
ENST00000583818.1:c.416+10C= ENSP00000461928.1:n.416+10C=
NM_207346.2:c.521+10C= NP_997229.2:n.521+10C=
XM_005257229.2:c.521+10C= XP_005257286.1:n.521+10C=
XM_006721821.2:c.218+10C= XP_006721884.1:n.218+10C=
XM_011524616.1:c.521+10C= XP_011522918.1:n.521+10C=
XM_011524617.1:c.521+10C= XP_011522919.1:n.521+10C=
XM_011524618.1:c.521+10C= XP_011522920.1:n.521+10C=
XR_243646.2:n.551+10C=
XM_005257229.4:c.521+10C= XP_005257286.1:n.521+10C=
XR_243646.4:n.557+10C=
NM_207346.3:c.521+10C= MANE Select NP_997229.2:n.521+10C=