Canonical Allele Identifier: CA365569008

Gene: TRDN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123570921A>T , CM000668.2:g.123570921A>T	GRCh38
NC_000006.11:g.123892066A>T , CM000668.1:g.123892066A>T	GRCh37
NC_000006.10:g.123933765A>T	NCBI36
NG_030438.1:g.71173T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361029.9:c.34+2T>A	ENSP00000354307.5:n.34+2T>A
ENST00000422596.2:c.34+2T>A	ENSP00000406768.2:n.34+2T>A
ENST00000546248.6:c.232+2T>A	ENSP00000439281.2:n.232+2T>A
ENST00000334268.9:c.232+2T>A MANE Select	ENSP00000333984.5:n.232+2T>A
ENST00000662930.1:c.232+2T>A	ENSP00000499585.1:n.232+2T>A
ENST00000334268.8:c.232+2T>A	ENSP00000333984.5:n.232+2T>A
ENST00000542443.5:c.232+2T>A	ENSP00000437684.1:n.232+2T>A
ENST00000546248.5:c.232+2T>A	ENSP00000439281.2:n.232+2T>A
ENST00000628709.2:c.232+2T>A	ENSP00000486095.1:n.232+2T>A
NM_001251987.1:c.232+2T>A	NP_001238916.1:n.232+2T>A
NM_001256020.1:c.232+2T>A	NP_001242949.1:n.232+2T>A
NM_001256021.1:c.232+2T>A	NP_001242950.1:n.232+2T>A
NM_001256022.1:c.232+2T>A	NP_001242951.1:n.232+2T>A
NM_006073.3:c.232+2T>A	NP_006064.2:n.232+2T>A
XM_011535382.1:c.232+2T>A	XP_011533684.1:n.232+2T>A
NM_006073.4:c.232+2T>A MANE Select	NP_006064.2:n.232+2T>A
NM_001251987.2:c.232+2T>A	NP_001238916.1:n.232+2T>A
NM_001256020.2:c.232+2T>A	NP_001242949.1:n.232+2T>A
NM_001256021.2:c.232+2T>A	NP_001242950.1:n.232+2T>A
NM_001256022.2:c.232+2T>A	NP_001242951.1:n.232+2T>A