Canonical Allele Identifier: CA3984250

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123497221G>A , CM000668.2:g.123497221G>A	GRCh38
NC_000006.11:g.123818366G>A , CM000668.1:g.123818366G>A	GRCh37
NC_000006.10:g.123860065G>A	NCBI36
NG_030438.1:g.144873C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.825C>T MANE Select	NP_006064.2:p.Asp275=
ENST00000334268.9:c.825C>T MANE Select	ENSP00000333984.5:p.Asp275=
NM_001251987.1:c.825C>T	NP_001238916.1:p.Asp275=
NM_001251987.2:c.825C>T	NP_001238916.1:p.Asp275=
NM_001256020.1:c.793+6498C>T	NP_001242949.1:n.793+6498C>T
NM_001256020.2:c.793+6498C>T	NP_001242949.1:n.793+6498C>T
NM_006073.3:c.825C>T	NP_006064.2:p.Asp275=
ENST00000334268.8:c.825C>T	ENSP00000333984.5:p.Asp275=
ENST00000361029.9:c.*1279C>T	ENSP00000354307.5:n.*1279C>T
ENST00000628709.2:c.793+6498C>T	ENSP00000486095.1:n.793+6498C>T
ENST00000662930.1:c.825C>T	ENSP00000499585.1:p.Asp275=
XM_011535382.1:c.825C>T	XP_011533684.1:p.Asp275=