Canonical Allele Identifier: CA2275548356
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516623C= , CM000679.2:g.75516623C= GRCh38
NC_000017.10:g.73512704C= , CM000679.1:g.73512704C= GRCh37
NC_000017.9:g.71024299C= NCBI36
NG_013041.1:g.5096C=
NG_033152.1:g.3961G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.56+7C= MANE Select ENSP00000327487.6:n.56+7C=
ENST00000434205.8:c.-83+237C= ENSP00000406559.4:n.-83+237C=
ENST00000545228.3:c.56+7C= ENSP00000438169.3:n.56+7C=
ENST00000579449.2:n.20+7C=
ENST00000580013.6:n.65+7C=
ENST00000583818.2:c.56+7C= ENSP00000461928.2:n.56+7C=
ENST00000679370.1:n.444-123C=
ENST00000679429.1:c.56+7C= ENSP00000505403.1:n.56+7C=
ENST00000679782.1:c.56+7C= ENSP00000505995.1:n.56+7C=
ENST00000679928.1:c.56+7C= ENSP00000506071.1:n.56+7C=
ENST00000680528.1:n.81+7C=
ENST00000680999.1:c.56+7C= ENSP00000504984.1:n.56+7C=
ENST00000681282.1:c.56+7C= ENSP00000506339.1:n.56+7C=
ENST00000333213.10:c.56+7C= ENSP00000327487.6:n.56+7C=
ENST00000434205.7:c.-83+237C= ENSP00000406559.3:n.-83+237C=
ENST00000580013.5:n.81+7C=
ENST00000583173.5:c.56+7C= ENSP00000463619.1:n.56+7C=
ENST00000583454.1:n.91+7C=
NM_207346.2:c.56+7C= NP_997229.2:n.56+7C=
XM_005257229.2:c.56+7C= XP_005257286.1:n.56+7C=
XM_006721821.2:c.-247-123C= XP_006721884.1:n.-247-123C=
XM_011524616.1:c.56+7C= XP_011522918.1:n.56+7C=
XM_011524617.1:c.56+7C= XP_011522919.1:n.56+7C=
XM_011524618.1:c.56+7C= XP_011522920.1:n.56+7C=
XR_243646.2:n.86+7C=
XM_005257229.4:c.56+7C= XP_005257286.1:n.56+7C=
XR_243646.4:n.92+7C=
NM_207346.3:c.56+7C= MANE Select NP_997229.2:n.56+7C=