Canonical Allele Identifier: CA3984390

Gene: TRDN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123547345T>C , CM000668.2:g.123547345T>C	GRCh38
NC_000006.11:g.123868490T>C , CM000668.1:g.123868490T>C	GRCh37
NC_000006.10:g.123910189T>C	NCBI36
NG_030438.1:g.94749A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361029.9:c.221A>G	ENSP00000354307.5:p.Lys74Arg
ENST00000422596.2:c.221A>G	ENSP00000406768.2:p.Lys74Arg
ENST00000546248.6:c.419A>G	ENSP00000439281.2:p.Lys140Arg
ENST00000334268.9:c.419A>G MANE Select	ENSP00000333984.5:p.Lys140Arg
ENST00000662930.1:c.419A>G	ENSP00000499585.1:p.Lys140Arg
ENST00000334268.8:c.419A>G	ENSP00000333984.5:p.Lys140Arg
ENST00000542443.5:c.419A>G	ENSP00000437684.1:p.Lys140Arg
ENST00000546248.5:c.419A>G	ENSP00000439281.2:p.Lys140Arg
ENST00000628709.2:c.419A>G	ENSP00000486095.1:p.Lys140Arg
NM_001251987.1:c.419A>G	NP_001238916.1:p.Lys140Arg
NM_001256020.1:c.419A>G	NP_001242949.1:p.Lys140Arg
NM_001256021.1:c.419A>G	NP_001242950.1:p.Lys140Arg
NM_001256022.1:c.419A>G	NP_001242951.1:p.Lys140Arg
NM_006073.3:c.419A>G	NP_006064.2:p.Lys140Arg
XM_011535382.1:c.419A>G	XP_011533684.1:p.Lys140Arg
XR_942945.1:n.2560-6011T>C
XR_001743830.1:n.1185-6011T>C
XR_001743831.1:n.3335-6011T>C
XR_001743832.1:n.3335-6011T>C
XR_001743833.1:n.2115-6011T>C
NM_006073.4:c.419A>G MANE Select	NP_006064.2:p.Lys140Arg
NM_001251987.2:c.419A>G	NP_001238916.1:p.Lys140Arg
NM_001256020.2:c.419A>G	NP_001242949.1:p.Lys140Arg
NM_001256021.2:c.419A>G	NP_001242950.1:p.Lys140Arg
NM_001256022.2:c.419A>G	NP_001242951.1:p.Lys140Arg