Canonical Allele Identifier: CA365564792

Gene: TRDN

Linked Data

• MyVariant Identifiers: chr6:g.123539877T>G (hg19) ; chr6:g.123218732T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218732T>G , CM000668.2:g.123218732T>G	GRCh38
NC_000006.11:g.123539877T>G , CM000668.1:g.123539877T>G	GRCh37
NC_000006.10:g.123581576T>G	NCBI36
NG_030438.1:g.423362A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2059A>C MANE Select	ENSP00000333984.5:p.Ser687Arg
ENST00000334268.8:c.2059A>C	ENSP00000333984.5:p.Ser687Arg
NM_006073.3:c.2059A>C	NP_006064.2:p.Ser687Arg
XM_011535382.1:c.1978A>C	XP_011533684.1:p.Ser660Arg
NM_006073.4:c.2059A>C MANE Select	NP_006064.2:p.Ser687Arg