Canonical Allele Identifier: CA3984523

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123636759G>A , CM000668.2:g.123636759G>A	GRCh38
NC_000006.11:g.123957904G>A , CM000668.1:g.123957904G>A	GRCh37
NC_000006.10:g.123999603G>A	NCBI36
NG_030438.1:g.5335C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.17C>T MANE Select	NP_006064.2:p.Ala6Val
ENST00000334268.9:c.17C>T MANE Select	ENSP00000333984.5:p.Ala6Val
NM_001251987.1:c.17C>T	NP_001238916.1:p.Ala6Val
NM_001251987.2:c.17C>T	NP_001238916.1:p.Ala6Val
NM_001256020.1:c.17C>T	NP_001242949.1:p.Ala6Val
NM_001256020.2:c.17C>T	NP_001242949.1:p.Ala6Val
NM_001256021.1:c.17C>T	NP_001242950.1:p.Ala6Val
NM_001256021.2:c.17C>T	NP_001242950.1:p.Ala6Val
NM_001256022.1:c.17C>T	NP_001242951.1:p.Ala6Val
NM_001256022.2:c.17C>T	NP_001242951.1:p.Ala6Val
NM_006073.3:c.17C>T	NP_006064.2:p.Ala6Val
ENST00000334268.8:c.17C>T	ENSP00000333984.5:p.Ala6Val
ENST00000542443.5:c.17C>T	ENSP00000437684.1:p.Ala6Val
ENST00000546248.5:c.17C>T	ENSP00000439281.2:p.Ala6Val
ENST00000546248.6:c.17C>T	ENSP00000439281.2:p.Ala6Val
ENST00000628709.2:c.17C>T	ENSP00000486095.1:p.Ala6Val
ENST00000662930.1:c.17C>T	ENSP00000499585.1:p.Ala6Val
XM_011535382.1:c.17C>T	XP_011533684.1:p.Ala6Val
XR_942943.1:n.72-18900G>A
XR_942943.2:n.1381-18900G>A