Canonical Allele Identifier: CA16612018

Gene: TRDN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123570988A>G , CM000668.2:g.123570988A>G	GRCh38
NC_000006.11:g.123892133A>G , CM000668.1:g.123892133A>G	GRCh37
NC_000006.10:g.123933832A>G	NCBI36
NG_030438.1:g.71106T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006073.4:c.167T>C MANE Select	NP_006064.2:p.Leu56Pro
ENST00000334268.9:c.167T>C MANE Select	ENSP00000333984.5:p.Leu56Pro
NM_001251987.1:c.167T>C	NP_001238916.1:p.Leu56Pro
NM_001251987.2:c.167T>C	NP_001238916.1:p.Leu56Pro
NM_001256020.1:c.167T>C	NP_001242949.1:p.Leu56Pro
NM_001256020.2:c.167T>C	NP_001242949.1:p.Leu56Pro
NM_001256021.1:c.167T>C	NP_001242950.1:p.Leu56Pro
NM_001256021.2:c.167T>C	NP_001242950.1:p.Leu56Pro
NM_001256022.1:c.167T>C	NP_001242951.1:p.Leu56Pro
NM_001256022.2:c.167T>C	NP_001242951.1:p.Leu56Pro
NM_006073.3:c.167T>C	NP_006064.2:p.Leu56Pro
ENST00000334268.8:c.167T>C	ENSP00000333984.5:p.Leu56Pro
ENST00000361029.9:c.-32T>C	ENSP00000354307.5:n.-32T>C
ENST00000422596.2:c.-32T>C	ENSP00000406768.2:n.-32T>C
ENST00000542443.5:c.167T>C	ENSP00000437684.1:p.Leu56Pro
ENST00000546248.5:c.167T>C	ENSP00000439281.2:p.Leu56Pro
ENST00000546248.6:c.167T>C	ENSP00000439281.2:p.Leu56Pro
ENST00000628709.2:c.167T>C	ENSP00000486095.1:p.Leu56Pro
ENST00000662930.1:c.167T>C	ENSP00000499585.1:p.Leu56Pro
XM_011535382.1:c.167T>C	XP_011533684.1:p.Leu56Pro