Canonical Allele Identifier: CA365568282

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123516189C>A , CM000668.2:g.123516189C>A	GRCh38
NC_000006.11:g.123837334C>A , CM000668.1:g.123837334C>A	GRCh37
NC_000006.10:g.123879033C>A	NCBI36
NG_030438.1:g.125905G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.502G>T MANE Select	NP_006064.2:p.Glu168Ter
ENST00000334268.9:c.502G>T MANE Select	ENSP00000333984.5:p.Glu168Ter
NM_001251987.1:c.502G>T	NP_001238916.1:p.Glu168Ter
NM_001251987.2:c.502G>T	NP_001238916.1:p.Glu168Ter
NM_001256020.1:c.502G>T	NP_001242949.1:p.Glu168Ter
NM_001256020.2:c.502G>T	NP_001242949.1:p.Glu168Ter
NM_001256021.1:c.502G>T	NP_001242950.1:p.Glu168Ter
NM_001256021.2:c.502G>T	NP_001242950.1:p.Glu168Ter
NM_006073.3:c.502G>T	NP_006064.2:p.Glu168Ter
ENST00000334268.8:c.502G>T	ENSP00000333984.5:p.Glu168Ter
ENST00000361029.8:c.18G>T
ENST00000361029.9:c.304G>T	ENSP00000354307.5:p.Glu102Ter
ENST00000546248.5:c.502G>T	ENSP00000439281.2:p.Glu168Ter
ENST00000546248.6:c.502G>T	ENSP00000439281.2:p.Glu168Ter
ENST00000628709.2:c.502G>T	ENSP00000486095.1:p.Glu168Ter
ENST00000662930.1:c.502G>T	ENSP00000499585.1:p.Glu168Ter
XM_011535382.1:c.502G>T	XP_011533684.1:p.Glu168Ter