Canonical Allele Identifier: CA365568467

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123530539G>A , CM000668.2:g.123530539G>A	GRCh38
NC_000006.11:g.123851684G>A , CM000668.1:g.123851684G>A	GRCh37
NC_000006.10:g.123893383G>A	NCBI36
NG_030438.1:g.111555C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.451C>T MANE Select	NP_006064.2:p.Gln151Ter
ENST00000334268.9:c.451C>T MANE Select	ENSP00000333984.5:p.Gln151Ter
NM_001251987.1:c.451C>T	NP_001238916.1:p.Gln151Ter
NM_001251987.2:c.451C>T	NP_001238916.1:p.Gln151Ter
NM_001256020.1:c.451C>T	NP_001242949.1:p.Gln151Ter
NM_001256020.2:c.451C>T	NP_001242949.1:p.Gln151Ter
NM_001256021.1:c.451C>T	NP_001242950.1:p.Gln151Ter
NM_001256021.2:c.451C>T	NP_001242950.1:p.Gln151Ter
NM_001256022.1:c.451C>T	NP_001242951.1:p.Gln151Ter
NM_001256022.2:c.451C>T	NP_001242951.1:p.Gln151Ter
NM_006073.3:c.451C>T	NP_006064.2:p.Gln151Ter
ENST00000334268.8:c.451C>T	ENSP00000333984.5:p.Gln151Ter
ENST00000361029.9:c.253C>T	ENSP00000354307.5:p.Gln85Ter
ENST00000422596.1:c.27C>T
ENST00000422596.2:c.253C>T	ENSP00000406768.2:p.Gln85Ter
ENST00000542443.5:c.451C>T	ENSP00000437684.1:p.Gln151Ter
ENST00000546248.5:c.451C>T	ENSP00000439281.2:p.Gln151Ter
ENST00000546248.6:c.451C>T	ENSP00000439281.2:p.Gln151Ter
ENST00000628709.2:c.451C>T	ENSP00000486095.1:p.Gln151Ter
ENST00000662930.1:c.451C>T	ENSP00000499585.1:p.Gln151Ter
XM_011535382.1:c.451C>T	XP_011533684.1:p.Gln151Ter
XR_001743833.1:n.1960-1067G>A
XR_942945.1:n.2171-1067G>A