Canonical Allele Identifier: CA3983850
Community Standard Title: NM_006073.4(TRDN):c.1593A>G (p.Lys531=)
Gene: TRDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123274645T>C , CM000668.2:g.123274645T>C GRCh38
NC_000006.11:g.123595790T>C , CM000668.1:g.123595790T>C GRCh37
NC_000006.10:g.123637489T>C NCBI36
NG_030438.1:g.367449A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006073.4:c.1593A>G MANE Select NP_006064.2:p.Lys531=
ENST00000334268.9:c.1593A>G MANE Select ENSP00000333984.5:p.Lys531=
NM_006073.3:c.1593A>G NP_006064.2:p.Lys531=
ENST00000334268.8:c.1593A>G ENSP00000333984.5:p.Lys531=
XM_011535382.1:c.1539A>G XP_011533684.1:p.Lys513=