Canonical Allele Identifier: CA365564645
Gene: TRDN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218697A>C , CM000668.2:g.123218697A>C GRCh38
NC_000006.11:g.123539842A>C , CM000668.1:g.123539842A>C GRCh37
NC_000006.10:g.123581541A>C NCBI36
NG_030438.1:g.423397T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2094T>G MANE Select ENSP00000333984.5:p.Asn698Lys
ENST00000334268.8:c.2094T>G ENSP00000333984.5:p.Asn698Lys
NM_006073.3:c.2094T>G NP_006064.2:p.Asn698Lys
XM_011535382.1:c.2013T>G XP_011533684.1:p.Asn671Lys
NM_006073.4:c.2094T>G MANE Select NP_006064.2:p.Asn698Lys