Canonical Allele Identifier: CA3223341985
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75523684C= , CM000679.2:g.75523684C= GRCh38
NC_000017.10:g.73519765C= , CM000679.1:g.73519765C= GRCh37
NC_000017.9:g.71031360C= NCBI36
NG_013041.1:g.12157C=

Transcript Alleles

HGVS Amino-acid Change
NM_207346.3:c.1335C= MANE Select NP_997229.2:p.Gly445=
ENST00000333213.11:c.1335C= MANE Select ENSP00000327487.6:p.Gly445=
NM_207346.2:c.1335C= NP_997229.2:p.Gly445=
ENST00000333213.10:c.1335C= ENSP00000327487.6:p.Gly445=
ENST00000434205.8:c.1032C= ENSP00000406559.4:p.Gly344=
ENST00000545228.2:c.612C=
ENST00000545228.3:c.1523C= ENSP00000438169.3:p.Ala508=
ENST00000577197.1:n.83C=
ENST00000577197.2:n.533C=
ENST00000579449.1:n.532C=
ENST00000579449.2:n.2075C=
ENST00000580013.6:n.2479C=
ENST00000679370.1:n.2857C=
ENST00000679429.1:c.*793C= ENSP00000505403.1:n.*793C=
ENST00000679443.1:n.1404C=
ENST00000679782.1:c.*34C= ENSP00000505995.1:n.*34C=
ENST00000679919.1:n.1606C=
ENST00000679928.1:c.*1887C= ENSP00000506071.1:n.*1887C=
ENST00000680528.1:n.2301C=
ENST00000680999.1:c.1548C= ENSP00000504984.1:p.Gly516=
ENST00000681282.1:c.*1522C= ENSP00000506339.1:n.*1522C=
XM_005257229.2:c.1523C= XP_005257286.1:p.Ala508=
XM_005257229.4:c.1523C= XP_005257286.1:p.Ala508=
XM_006721821.2:c.1220C= XP_006721884.1:p.Ala407=
XM_011524616.1:c.1501+349C= XP_011522918.1:n.1501+349C=
XM_011524617.1:c.*12+349C= XP_011522919.1:n.*12+349C=
XM_011524618.1:c.1313+349C= XP_011522920.1:n.1313+349C=
XR_001753015.1:n.88-316G=
XR_001753016.1:n.89-280G=
XR_243646.2:n.1567C=
XR_243646.4:n.1573C=