Canonical Allele Identifier: CA1660320206
Gene: TRDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218778G= , CM000668.2:g.123218778G= GRCh38
NC_000006.11:g.123539923G= , CM000668.1:g.123539923G= GRCh37
NC_000006.10:g.123581622G= NCBI36
NG_030438.1:g.423316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2051-38C= MANE Select ENSP00000333984.5:n.2051-38C=
ENST00000334268.8:c.2051-38C= ENSP00000333984.5:n.2051-38C=
NM_006073.3:c.2051-38C= NP_006064.2:n.2051-38C=
XM_011535382.1:c.1970-38C= XP_011533684.1:n.1970-38C=
NM_006073.4:c.2051-38C= MANE Select NP_006064.2:n.2051-38C=