Canonical Allele Identifier: CA365564465

Gene: TRDN

Linked Data

• MyVariant Identifiers: chr6:g.123539792C>G (hg19) ; chr6:g.123218647C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218647C>G , CM000668.2:g.123218647C>G	GRCh38
NC_000006.11:g.123539792C>G , CM000668.1:g.123539792C>G	GRCh37
NC_000006.10:g.123581491C>G	NCBI36
NG_030438.1:g.423447G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2144G>C MANE Select	ENSP00000333984.5:p.Ser715Thr
ENST00000334268.8:c.2144G>C	ENSP00000333984.5:p.Ser715Thr
NM_006073.3:c.2144G>C	NP_006064.2:p.Ser715Thr
XM_011535382.1:c.2063G>C	XP_011533684.1:p.Ser688Thr
NM_006073.4:c.2144G>C MANE Select	NP_006064.2:p.Ser715Thr