Canonical Allele Identifier: CA2275551155
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521667_75521668delinsCA , CM000679.2:g.75521667_75521668delinsCA GRCh38
NC_000017.10:g.73517748_73517749delinsCA , CM000679.1:g.73517748_73517749delinsCA GRCh37
NC_000017.9:g.71029343_71029344delinsCA NCBI36
NG_013041.1:g.10140_10141delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.624-38_624-37delinsCA MANE Select ENSP00000327487.6:n.624-38_624-37delinsCA
ENST00000434205.8:c.321-38_321-37delinsCA ENSP00000406559.4:n.321-38_321-37delinsCA
ENST00000545228.3:c.624-38_624-37delinsCA ENSP00000438169.3:n.624-38_624-37delinsCA
ENST00000579449.2:n.423-38_423-37delinsCA
ENST00000580013.6:n.789_790delinsCA
ENST00000583818.2:c.678-38_678-37delinsCA ENSP00000461928.2:n.678-38_678-37delinsCA
ENST00000679370.1:n.1167_1168delinsCA
ENST00000679429.1:c.*82-38_*82-37delinsCA ENSP00000505403.1:n.*82-38_*82-37delinsCA
ENST00000679443.1:n.655_656delinsCA
ENST00000679782.1:c.624-38_624-37delinsCA ENSP00000505995.1:n.624-38_624-37delinsCA
ENST00000679919.1:n.655_656delinsCA
ENST00000679928.1:c.*235-38_*235-37delinsCA ENSP00000506071.1:n.*235-38_*235-37delinsCA
ENST00000680528.1:n.649-38_649-37delinsCA
ENST00000680999.1:c.624-38_624-37delinsCA ENSP00000504984.1:n.624-38_624-37delinsCA
ENST00000681282.1:c.624-9_624-8delinsCA ENSP00000506339.1:n.624-9_624-8delinsCA
ENST00000333213.10:c.624-38_624-37delinsCA ENSP00000327487.6:n.624-38_624-37delinsCA
ENST00000578415.1:c.584-38_584-37delinsCA
ENST00000583173.5:c.458+157_458+158delinsCA ENSP00000463619.1:n.458+157_458+158delinsCA
ENST00000583818.1:c.573-38_573-37delinsCA ENSP00000461928.1:n.573-38_573-37delinsCA
NM_207346.2:c.624-38_624-37delinsCA NP_997229.2:n.624-38_624-37delinsCA
XM_005257229.2:c.624-38_624-37delinsCA XP_005257286.1:n.624-38_624-37delinsCA
XM_006721821.2:c.321-38_321-37delinsCA XP_006721884.1:n.321-38_321-37delinsCA
XM_011524616.1:c.624-38_624-37delinsCA XP_011522918.1:n.624-38_624-37delinsCA
XM_011524617.1:c.624-38_624-37delinsCA XP_011522919.1:n.624-38_624-37delinsCA
XM_011524618.1:c.624-38_624-37delinsCA XP_011522920.1:n.624-38_624-37delinsCA
XR_243646.2:n.654-38_654-37delinsCA
XM_005257229.4:c.624-38_624-37delinsCA XP_005257286.1:n.624-38_624-37delinsCA
XR_243646.4:n.660-38_660-37delinsCA
NM_207346.3:c.624-38_624-37delinsCA MANE Select NP_997229.2:n.624-38_624-37delinsCA