Canonical Allele Identifier: CA365564571

Gene: TRDN

Linked Data

• MyVariant Identifiers: chr6:g.123539825A>C (hg19) ; chr6:g.123218680A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218680A>C , CM000668.2:g.123218680A>C	GRCh38
NC_000006.11:g.123539825A>C , CM000668.1:g.123539825A>C	GRCh37
NC_000006.10:g.123581524A>C	NCBI36
NG_030438.1:g.423414T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2111T>G MANE Select	ENSP00000333984.5:p.Phe704Cys
ENST00000334268.8:c.2111T>G	ENSP00000333984.5:p.Phe704Cys
NM_006073.3:c.2111T>G	NP_006064.2:p.Phe704Cys
XM_011535382.1:c.2030T>G	XP_011533684.1:p.Phe677Cys
NM_006073.4:c.2111T>G MANE Select	NP_006064.2:p.Phe704Cys