Canonical Allele Identifier: CA3984255

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123497249T>C , CM000668.2:g.123497249T>C	GRCh38
NC_000006.11:g.123818394T>C , CM000668.1:g.123818394T>C	GRCh37
NC_000006.10:g.123860093T>C	NCBI36
NG_030438.1:g.144845A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.797A>G MANE Select	NP_006064.2:p.Gln266Arg
ENST00000334268.9:c.797A>G MANE Select	ENSP00000333984.5:p.Gln266Arg
NM_001251987.1:c.797A>G	NP_001238916.1:p.Gln266Arg
NM_001251987.2:c.797A>G	NP_001238916.1:p.Gln266Arg
NM_001256020.1:c.793+6470A>G	NP_001242949.1:n.793+6470A>G
NM_001256020.2:c.793+6470A>G	NP_001242949.1:n.793+6470A>G
NM_006073.3:c.797A>G	NP_006064.2:p.Gln266Arg
ENST00000334268.8:c.797A>G	ENSP00000333984.5:p.Gln266Arg
ENST00000361029.9:c.*1251A>G	ENSP00000354307.5:n.*1251A>G
ENST00000628709.2:c.793+6470A>G	ENSP00000486095.1:n.793+6470A>G
ENST00000662930.1:c.797A>G	ENSP00000499585.1:p.Gln266Arg
XM_011535382.1:c.797A>G	XP_011533684.1:p.Gln266Arg