Canonical Allele Identifier: CA1660507688

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123599427T= , CM000668.2:g.123599427T=	GRCh38
NC_000006.11:g.123920572T= , CM000668.1:g.123920572T=	GRCh37
NC_000006.10:g.123962271T=	NCBI36
NG_030438.1:g.42667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546248.6:c.23-28295A=	ENSP00000439281.2:n.23-28295A=
ENST00000334268.9:c.23-28295A= MANE Select	ENSP00000333984.5:n.23-28295A=
ENST00000662930.1:c.23-28295A=	ENSP00000499585.1:n.23-28295A=
ENST00000334268.8:c.23-28295A=	ENSP00000333984.5:n.23-28295A=
ENST00000542443.5:c.23-28295A=	ENSP00000437684.1:n.23-28295A=
ENST00000546248.5:c.23-28295A=	ENSP00000439281.2:n.23-28295A=
ENST00000628709.2:c.23-28295A=	ENSP00000486095.1:n.23-28295A=
NM_001251987.1:c.23-28295A=	NP_001238916.1:n.23-28295A=
NM_001256020.1:c.23-28295A=	NP_001242949.1:n.23-28295A=
NM_001256021.1:c.23-28295A=	NP_001242950.1:n.23-28295A=
NM_001256022.1:c.23-28295A=	NP_001242951.1:n.23-28295A=
NM_006073.3:c.23-28295A=	NP_006064.2:n.23-28295A=
XM_011535382.1:c.23-28295A=	XP_011533684.1:n.23-28295A=
NM_006073.4:c.23-28295A= MANE Select	NP_006064.2:n.23-28295A=
NM_001251987.2:c.23-28295A=	NP_001238916.1:n.23-28295A=
NM_001256020.2:c.23-28295A=	NP_001242949.1:n.23-28295A=
NM_001256021.2:c.23-28295A=	NP_001242950.1:n.23-28295A=
NM_001256022.2:c.23-28295A=	NP_001242951.1:n.23-28295A=