Canonical Allele Identifier: CA2639833549
Gene: TSEN54 HGNC NCBI

Linked Data

gnomAD v4: 17-75516165-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516165C>A , CM000679.2:g.75516165C>A GRCh38
NC_000017.10:g.73512246C>A , CM000679.1:g.73512246C>A GRCh37
NC_000017.9:g.71023841C>A NCBI36
NG_013041.1:g.4638C>A
NG_033152.1:g.4419G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-304C>A ENSP00000406559.4:n.-304C>A
ENST00000679370.1:n.222C>A
ENST00000434205.7:c.-304C>A ENSP00000406559.3:n.-304C>A
XM_006721821.2:c.-469C>A XP_006721884.1:n.-469C>A
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