Canonical Allele Identifier: CA1618634804

Gene: TRIM26

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30211645G= , CM000668.2:g.30211645G=	GRCh38
NC_000006.11:g.30179422G= , CM000668.1:g.30179422G=	GRCh37
NC_000006.10:g.30287401G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003449.5:c.-376+1660C= MANE Select	NP_003440.1:n.-376+1660C=
ENST00000454678.7:c.-376+1660C= MANE Select	ENSP00000410446.2:n.-376+1660C=
NM_001242783.1:c.-155+1660C=	NP_001229712.1:n.-155+1660C=
NM_001242783.2:c.-155+1660C=	NP_001229712.1:n.-155+1660C=
NM_003449.4:c.-376+1660C=	NP_003440.1:n.-376+1660C=
ENST00000416596.5:c.-265+1660C=	ENSP00000413673.1:n.-265+1660C=
ENST00000418026.1:c.-51+1660C=	ENSP00000387530.1:n.-51+1660C=
ENST00000434785.5:c.-155+1660C=	ENSP00000400920.1:n.-155+1660C=
ENST00000453195.5:c.-155+1660C=	ENSP00000391879.1:n.-155+1660C=
ENST00000454678.6:c.-376+1660C=	ENSP00000410446.2:n.-376+1660C=
ENST00000487829.1:n.61+1660C=
XM_005249374.2:c.-265+1660C=	XP_005249431.1:n.-265+1660C=
XM_005249375.2:c.-250+1660C=	XP_005249432.1:n.-250+1660C=
XM_005249376.2:c.-361+1660C=	XP_005249433.1:n.-361+1660C=
XM_005249377.2:c.-140+1660C=	XP_005249434.1:n.-140+1660C=
XM_005249378.2:c.-51+1660C=	XP_005249435.1:n.-51+1660C=
XM_006715180.2:c.-266+1660C=	XP_006715243.1:n.-266+1660C=
XM_011514859.1:c.-265+1660C=	XP_011513161.1:n.-265+1660C=
XM_017011263.1:c.-155+1660C=	XP_016866752.1:n.-155+1660C=