Canonical Allele Identifier: CA1660320218

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218800T= , CM000668.2:g.123218800T=	GRCh38
NC_000006.11:g.123539945T= , CM000668.1:g.123539945T=	GRCh37
NC_000006.10:g.123581644T=	NCBI36
NG_030438.1:g.423294A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2051-60A= MANE Select	ENSP00000333984.5:n.2051-60A=
ENST00000334268.8:c.2051-60A=	ENSP00000333984.5:n.2051-60A=
NM_006073.3:c.2051-60A=	NP_006064.2:n.2051-60A=
XM_011535382.1:c.1970-60A=	XP_011533684.1:n.1970-60A=
NM_006073.4:c.2051-60A= MANE Select	NP_006064.2:n.2051-60A=