Canonical Allele Identifier: CA775074835
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs1252610427

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75518746dup , CM000679.2:g.75518746dup GRCh38
NC_000017.10:g.73514827dup , CM000679.1:g.73514827dup GRCh37
NC_000017.9:g.71026422dup NCBI36
NG_013041.1:g.7219dup
NG_033152.1:g.1838dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.469-249dup MANE Select ENSP00000327487.6:n.469-249dup
ENST00000434205.8:c.166-249dup ENSP00000406559.4:n.166-249dup
ENST00000545228.3:c.469-249dup ENSP00000438169.3:n.469-249dup
ENST00000579449.2:n.268-249dup
ENST00000580013.6:n.478-249dup
ENST00000583818.2:c.469-249dup ENSP00000461928.2:n.469-249dup
ENST00000679370.1:n.856-249dup
ENST00000679429.1:c.469-257dup ENSP00000505403.1:n.469-257dup
ENST00000679443.1:n.344-249dup
ENST00000679782.1:c.469-249dup ENSP00000505995.1:n.469-249dup
ENST00000679919.1:n.344-249dup
ENST00000679928.1:c.469-249dup ENSP00000506071.1:n.469-249dup
ENST00000680528.1:n.494-249dup
ENST00000680999.1:c.469-249dup ENSP00000504984.1:n.469-249dup
ENST00000681282.1:c.469-249dup ENSP00000506339.1:n.469-249dup
ENST00000333213.10:c.469-249dup ENSP00000327487.6:n.469-249dup
ENST00000434205.7:c.166-249dup ENSP00000406559.3:n.166-249dup
ENST00000578415.1:c.429-249dup
ENST00000580013.5:n.494-257dup
ENST00000583173.5:c.304-249dup ENSP00000463619.1:n.304-249dup
ENST00000583818.1:c.364-249dup ENSP00000461928.1:n.364-249dup
NM_207346.2:c.469-249dup NP_997229.2:n.469-249dup
XM_005257229.2:c.469-249dup XP_005257286.1:n.469-249dup
XM_006721821.2:c.166-249dup XP_006721884.1:n.166-249dup
XM_011524616.1:c.469-249dup XP_011522918.1:n.469-249dup
XM_011524617.1:c.469-249dup XP_011522919.1:n.469-249dup
XM_011524618.1:c.469-249dup XP_011522920.1:n.469-249dup
XR_243646.2:n.499-249dup
XM_005257229.4:c.469-249dup XP_005257286.1:n.469-249dup
XR_243646.4:n.505-249dup
NM_207346.3:c.469-249dup MANE Select NP_997229.2:n.469-249dup