Canonical Allele Identifier: CA2275551184
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521718A= , CM000679.2:g.75521718A= GRCh38
NC_000017.10:g.73517799A= , CM000679.1:g.73517799A= GRCh37
NC_000017.9:g.71029394A= NCBI36
NG_013041.1:g.10191A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.637A= MANE Select ENSP00000327487.6:p.Lys213=
ENST00000434205.8:c.334A= ENSP00000406559.4:p.Lys112=
ENST00000545228.3:c.637A= ENSP00000438169.3:p.Lys213=
ENST00000579449.2:n.436A=
ENST00000580013.6:n.840A=
ENST00000583818.2:c.691A= ENSP00000461928.2:n.691A=
ENST00000679370.1:n.1218A=
ENST00000679429.1:c.*95A= ENSP00000505403.1:n.*95A=
ENST00000679443.1:n.706A=
ENST00000679782.1:c.637A= ENSP00000505995.1:p.Lys213=
ENST00000679919.1:n.706A=
ENST00000679928.1:c.*248A= ENSP00000506071.1:n.*248A=
ENST00000680528.1:n.662A=
ENST00000680999.1:c.637A= ENSP00000504984.1:p.Lys213=
ENST00000681282.1:c.666A= ENSP00000506339.1:p.Arg222=
ENST00000333213.10:c.637A= ENSP00000327487.6:p.Lys213=
ENST00000578415.1:c.597A=
ENST00000583173.5:c.458+208A= ENSP00000463619.1:n.458+208A=
ENST00000583818.1:c.586A= ENSP00000461928.1:n.586A=
NM_207346.2:c.637A= NP_997229.2:p.Lys213=
XM_005257229.2:c.637A= XP_005257286.1:p.Lys213=
XM_006721821.2:c.334A= XP_006721884.1:p.Lys112=
XM_011524616.1:c.637A= XP_011522918.1:p.Lys213=
XM_011524617.1:c.637A= XP_011522919.1:p.Lys213=
XM_011524618.1:c.637A= XP_011522920.1:p.Lys213=
XR_243646.2:n.667A=
XM_005257229.4:c.637A= XP_005257286.1:p.Lys213=
XR_243646.4:n.673A=
NM_207346.3:c.637A= MANE Select NP_997229.2:p.Lys213=