Canonical Allele Identifier: CA2581556274

Gene: TRIM26

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30185184T>G , CM000668.2:g.30185184T>G	GRCh38
NC_000006.11:g.30152961T>G , CM000668.1:g.30152961T>G	GRCh37
NC_000006.10:g.30260940T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003449.5:c.*692A>C MANE Select	NP_003440.1:n.*692A>C
ENST00000454678.7:c.*692A>C MANE Select	ENSP00000410446.2:n.*692A>C
NM_001242783.1:c.*692A>C	NP_001229712.1:n.*692A>C
NM_001242783.2:c.*692A>C	NP_001229712.1:n.*692A>C
NM_003449.4:c.*692A>C	NP_003440.1:n.*692A>C
ENST00000437089.5:c.*692A>C	ENSP00000395491.1:n.*692A>C
ENST00000453195.5:c.*692A>C	ENSP00000391879.1:n.*692A>C
ENST00000454678.6:c.*692A>C	ENSP00000410446.2:n.*692A>C
ENST00000480999.1:n.2385A>C
XM_005249374.2:c.*692A>C	XP_005249431.1:n.*692A>C
XM_005249375.2:c.*692A>C	XP_005249432.1:n.*692A>C
XM_005249376.2:c.*692A>C	XP_005249433.1:n.*692A>C
XM_005249377.2:c.*692A>C	XP_005249434.1:n.*692A>C
XM_005249378.2:c.*692A>C	XP_005249435.1:n.*692A>C
XM_006715180.2:c.*692A>C	XP_006715243.1:n.*692A>C
XM_011514859.1:c.*692A>C	XP_011513161.1:n.*692A>C
XM_017011263.1:c.*692A>C	XP_016866752.1:n.*692A>C