Canonical Allele Identifier: CA1660320203
Gene: TRDN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218774T= , CM000668.2:g.123218774T= GRCh38
NC_000006.11:g.123539919T= , CM000668.1:g.123539919T= GRCh37
NC_000006.10:g.123581618T= NCBI36
NG_030438.1:g.423320A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2051-34A= MANE Select ENSP00000333984.5:n.2051-34A=
ENST00000334268.8:c.2051-34A= ENSP00000333984.5:n.2051-34A=
NM_006073.3:c.2051-34A= NP_006064.2:n.2051-34A=
XM_011535382.1:c.1970-34A= XP_011533684.1:n.1970-34A=
NM_006073.4:c.2051-34A= MANE Select NP_006064.2:n.2051-34A=
Search 100 bp 5'
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