Canonical Allele Identifier: CA365568634

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123548453C>T , CM000668.2:g.123548453C>T	GRCh38
NC_000006.11:g.123869598C>T , CM000668.1:g.123869598C>T	GRCh37
NC_000006.10:g.123911297C>T	NCBI36
NG_030438.1:g.93641G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.391+1G>A MANE Select	NP_006064.2:n.391+1G>A
ENST00000334268.9:c.391+1G>A MANE Select	ENSP00000333984.5:n.391+1G>A
NM_001251987.1:c.391+1G>A	NP_001238916.1:n.391+1G>A
NM_001251987.2:c.391+1G>A	NP_001238916.1:n.391+1G>A
NM_001256020.1:c.391+1G>A	NP_001242949.1:n.391+1G>A
NM_001256020.2:c.391+1G>A	NP_001242949.1:n.391+1G>A
NM_001256021.1:c.391+1G>A	NP_001242950.1:n.391+1G>A
NM_001256021.2:c.391+1G>A	NP_001242950.1:n.391+1G>A
NM_001256022.1:c.391+1G>A	NP_001242951.1:n.391+1G>A
NM_001256022.2:c.391+1G>A	NP_001242951.1:n.391+1G>A
NM_006073.3:c.391+1G>A	NP_006064.2:n.391+1G>A
ENST00000334268.8:c.391+1G>A	ENSP00000333984.5:n.391+1G>A
ENST00000361029.9:c.193+1G>A	ENSP00000354307.5:n.193+1G>A
ENST00000422596.2:c.193+1G>A	ENSP00000406768.2:n.193+1G>A
ENST00000542443.5:c.391+1G>A	ENSP00000437684.1:n.391+1G>A
ENST00000546248.5:c.391+1G>A	ENSP00000439281.2:n.391+1G>A
ENST00000546248.6:c.391+1G>A	ENSP00000439281.2:n.391+1G>A
ENST00000628709.2:c.391+1G>A	ENSP00000486095.1:n.391+1G>A
ENST00000662930.1:c.391+1G>A	ENSP00000499585.1:n.391+1G>A
XM_011535382.1:c.391+1G>A	XP_011533684.1:n.391+1G>A
XR_001743830.1:n.1185-4903C>T
XR_001743831.1:n.3335-4903C>T
XR_001743832.1:n.3335-4903C>T
XR_001743833.1:n.2115-4903C>T
XR_942945.1:n.2560-4903C>T