Canonical Allele Identifier: CA3984519

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123636725T>C , CM000668.2:g.123636725T>C	GRCh38
NC_000006.11:g.123957870T>C , CM000668.1:g.123957870T>C	GRCh37
NC_000006.10:g.123999569T>C	NCBI36
NG_030438.1:g.5369A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.22+29A>G MANE Select	NP_006064.2:n.22+29A>G
ENST00000334268.9:c.22+29A>G MANE Select	ENSP00000333984.5:n.22+29A>G
NM_001251987.1:c.22+29A>G	NP_001238916.1:n.22+29A>G
NM_001251987.2:c.22+29A>G	NP_001238916.1:n.22+29A>G
NM_001256020.1:c.22+29A>G	NP_001242949.1:n.22+29A>G
NM_001256020.2:c.22+29A>G	NP_001242949.1:n.22+29A>G
NM_001256021.1:c.22+29A>G	NP_001242950.1:n.22+29A>G
NM_001256021.2:c.22+29A>G	NP_001242950.1:n.22+29A>G
NM_001256022.1:c.22+29A>G	NP_001242951.1:n.22+29A>G
NM_001256022.2:c.22+29A>G	NP_001242951.1:n.22+29A>G
NM_006073.3:c.22+29A>G	NP_006064.2:n.22+29A>G
ENST00000334268.8:c.22+29A>G	ENSP00000333984.5:n.22+29A>G
ENST00000542443.5:c.22+29A>G	ENSP00000437684.1:n.22+29A>G
ENST00000546248.5:c.22+29A>G	ENSP00000439281.2:n.22+29A>G
ENST00000546248.6:c.22+29A>G	ENSP00000439281.2:n.22+29A>G
ENST00000628709.2:c.22+29A>G	ENSP00000486095.1:n.22+29A>G
ENST00000662930.1:c.22+29A>G	ENSP00000499585.1:n.22+29A>G
XM_011535382.1:c.22+29A>G	XP_011533684.1:n.22+29A>G
XR_942943.1:n.72-18934T>C
XR_942943.2:n.1381-18934T>C