Canonical Allele Identifier: CA401028182
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521425T>G , CM000679.2:g.75521425T>G GRCh38
NC_000017.10:g.73517506T>G , CM000679.1:g.73517506T>G GRCh37
NC_000017.9:g.71029101T>G NCBI36
NG_013041.1:g.9898T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.538T>G MANE Select ENSP00000327487.6:p.Tyr180Asp
ENST00000434205.8:c.235T>G ENSP00000406559.4:p.Tyr79Asp
ENST00000545228.3:c.538T>G ENSP00000438169.3:p.Tyr180Asp
ENST00000579449.2:n.337T>G
ENST00000580013.6:n.547T>G
ENST00000583818.2:c.592T>G ENSP00000461928.2:n.592T>G
ENST00000679370.1:n.925T>G
ENST00000679429.1:c.530T>G ENSP00000505403.1:p.Val177Gly
ENST00000679443.1:n.413T>G
ENST00000679782.1:c.538T>G ENSP00000505995.1:p.Tyr180Asp
ENST00000679919.1:n.413T>G
ENST00000679928.1:c.*149T>G ENSP00000506071.1:n.*149T>G
ENST00000680528.1:n.563T>G
ENST00000680999.1:c.538T>G ENSP00000504984.1:p.Tyr180Asp
ENST00000681282.1:c.538T>G ENSP00000506339.1:p.Tyr180Asp
ENST00000333213.10:c.538T>G ENSP00000327487.6:p.Tyr180Asp
ENST00000578415.1:c.498T>G
ENST00000580013.5:n.555T>G
ENST00000583173.5:c.373T>G ENSP00000463619.1:p.Tyr125Asp
ENST00000583818.1:c.487T>G ENSP00000461928.1:n.487T>G
NM_207346.2:c.538T>G NP_997229.2:p.Tyr180Asp
XM_005257229.2:c.538T>G XP_005257286.1:p.Tyr180Asp
XM_006721821.2:c.235T>G XP_006721884.1:p.Tyr79Asp
XM_011524616.1:c.538T>G XP_011522918.1:p.Tyr180Asp
XM_011524617.1:c.538T>G XP_011522919.1:p.Tyr180Asp
XM_011524618.1:c.538T>G XP_011522920.1:p.Tyr180Asp
XR_243646.2:n.568T>G
XM_005257229.4:c.538T>G XP_005257286.1:p.Tyr180Asp
XR_243646.4:n.574T>G
NM_207346.3:c.538T>G MANE Select NP_997229.2:p.Tyr180Asp