Canonical Allele Identifier: CA1660320168

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218708C= , CM000668.2:g.123218708C=	GRCh38
NC_000006.11:g.123539853C= , CM000668.1:g.123539853C=	GRCh37
NC_000006.10:g.123581552C=	NCBI36
NG_030438.1:g.423386G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2083G= MANE Select	ENSP00000333984.5:p.Asp695=
ENST00000334268.8:c.2083G=	ENSP00000333984.5:p.Asp695=
NM_006073.3:c.2083G=	NP_006064.2:p.Asp695=
XM_011535382.1:c.2002G=	XP_011533684.1:p.Asp668=
NM_006073.4:c.2083G= MANE Select	NP_006064.2:p.Asp695=