Canonical Allele Identifier: CA365567076
Community Standard Title: NM_006073.4(TRDN):c.1115A>G (p.Lys372Arg)
Gene: TRDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123388542T>C , CM000668.2:g.123388542T>C GRCh38
NC_000006.11:g.123709687T>C , CM000668.1:g.123709687T>C GRCh37
NC_000006.10:g.123751386T>C NCBI36
NG_030438.1:g.253552A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006073.4:c.1115A>G MANE Select NP_006064.2:p.Lys372Arg
ENST00000334268.9:c.1115A>G MANE Select ENSP00000333984.5:p.Lys372Arg
NM_001251987.1:c.1118A>G NP_001238916.1:p.Lys373Arg
NM_001251987.2:c.1118A>G NP_001238916.1:p.Lys373Arg
NM_006073.3:c.1115A>G NP_006064.2:p.Lys372Arg
ENST00000334268.8:c.1115A>G ENSP00000333984.5:p.Lys372Arg
ENST00000662930.1:c.1118A>G ENSP00000499585.1:p.Lys373Arg
XM_011535382.1:c.1115A>G XP_011533684.1:p.Lys372Arg