Canonical Allele Identifier: CA365564569

Gene: TRDN

Linked Data

• MyVariant Identifiers: chr6:g.123539824A>T (hg19) ; chr6:g.123218679A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218679A>T , CM000668.2:g.123218679A>T	GRCh38
NC_000006.11:g.123539824A>T , CM000668.1:g.123539824A>T	GRCh37
NC_000006.10:g.123581523A>T	NCBI36
NG_030438.1:g.423415T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2112T>A MANE Select	ENSP00000333984.5:p.Phe704Leu
ENST00000334268.8:c.2112T>A	ENSP00000333984.5:p.Phe704Leu
NM_006073.3:c.2112T>A	NP_006064.2:p.Phe704Leu
XM_011535382.1:c.2031T>A	XP_011533684.1:p.Phe677Leu
NM_006073.4:c.2112T>A MANE Select	NP_006064.2:p.Phe704Leu