Canonical Allele Identifier: CA365567962

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123636753C>A , CM000668.2:g.123636753C>A	GRCh38
NC_000006.11:g.123957898C>A , CM000668.1:g.123957898C>A	GRCh37
NC_000006.10:g.123999597C>A	NCBI36
NG_030438.1:g.5341G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.22+1G>T MANE Select	NP_006064.2:n.22+1G>T
ENST00000334268.9:c.22+1G>T MANE Select	ENSP00000333984.5:n.22+1G>T
NM_001251987.1:c.22+1G>T	NP_001238916.1:n.22+1G>T
NM_001251987.2:c.22+1G>T	NP_001238916.1:n.22+1G>T
NM_001256020.1:c.22+1G>T	NP_001242949.1:n.22+1G>T
NM_001256020.2:c.22+1G>T	NP_001242949.1:n.22+1G>T
NM_001256021.1:c.22+1G>T	NP_001242950.1:n.22+1G>T
NM_001256021.2:c.22+1G>T	NP_001242950.1:n.22+1G>T
NM_001256022.1:c.22+1G>T	NP_001242951.1:n.22+1G>T
NM_001256022.2:c.22+1G>T	NP_001242951.1:n.22+1G>T
NM_006073.3:c.22+1G>T	NP_006064.2:n.22+1G>T
ENST00000334268.8:c.22+1G>T	ENSP00000333984.5:n.22+1G>T
ENST00000542443.5:c.22+1G>T	ENSP00000437684.1:n.22+1G>T
ENST00000546248.5:c.22+1G>T	ENSP00000439281.2:n.22+1G>T
ENST00000546248.6:c.22+1G>T	ENSP00000439281.2:n.22+1G>T
ENST00000628709.2:c.22+1G>T	ENSP00000486095.1:n.22+1G>T
ENST00000662930.1:c.22+1G>T	ENSP00000499585.1:n.22+1G>T
XM_011535382.1:c.22+1G>T	XP_011533684.1:n.22+1G>T
XR_942943.1:n.72-18906C>A
XR_942943.2:n.1381-18906C>A