Canonical Allele Identifier: CA1660320176
Gene: TRDN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218721C= , CM000668.2:g.123218721C= GRCh38
NC_000006.11:g.123539866C= , CM000668.1:g.123539866C= GRCh37
NC_000006.10:g.123581565C= NCBI36
NG_030438.1:g.423373G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2070G= MANE Select ENSP00000333984.5:p.Gln690=
ENST00000334268.8:c.2070G= ENSP00000333984.5:p.Gln690=
NM_006073.3:c.2070G= NP_006064.2:p.Gln690=
XM_011535382.1:c.1989G= XP_011533684.1:p.Gln663=
NM_006073.4:c.2070G= MANE Select NP_006064.2:p.Gln690=
Search 100 bp 5'
Search 100 bp 3'