Canonical Allele Identifier: CA12230275

Gene: TRIM26

Linked Data

• dbSNP Id: rs2021722
• gnomAD v2: 6-30174131-C-T
• gnomAD v3: 6-30206354-C-T
• gnomAD v4: 6-30206354-C-T
• MyVariant Identifiers: chr6:g.30174131C>T (hg19) ; chr6:g.30206354C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30206354C>T , CM000668.2:g.30206354C>T	GRCh38
NC_000006.11:g.30174131C>T , CM000668.1:g.30174131C>T	GRCh37
NC_000006.10:g.30282110C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454678.7:c.-375-1589G>A MANE Select	ENSP00000410446.2:n.-375-1589G>A
ENST00000416596.5:c.-264-1589G>A	ENSP00000413673.1:n.-264-1589G>A
ENST00000418026.1:c.-51+6951G>A	ENSP00000387530.1:n.-51+6951G>A
ENST00000434785.5:c.-154-1589G>A	ENSP00000400920.1:n.-154-1589G>A
ENST00000453195.5:c.-154-5216G>A	ENSP00000391879.1:n.-154-5216G>A
ENST00000454678.6:c.-375-1589G>A	ENSP00000410446.2:n.-375-1589G>A
ENST00000487829.1:n.62-1589G>A
NM_001242783.1:c.-154-5216G>A	NP_001229712.1:n.-154-5216G>A
NM_003449.4:c.-375-1589G>A	NP_003440.1:n.-375-1589G>A
XM_005249374.2:c.-264-1589G>A	XP_005249431.1:n.-264-1589G>A
XM_005249375.2:c.-249-1589G>A	XP_005249432.1:n.-249-1589G>A
XM_005249376.2:c.-360-1589G>A	XP_005249433.1:n.-360-1589G>A
XM_005249377.2:c.-139-5231G>A	XP_005249434.1:n.-139-5231G>A
XM_005249378.2:c.-51+6951G>A	XP_005249435.1:n.-51+6951G>A
XM_006715180.2:c.-265-5216G>A	XP_006715243.1:n.-265-5216G>A
XM_011514859.1:c.-264-1589G>A	XP_011513161.1:n.-264-1589G>A
XM_017011263.1:c.-154-5216G>A	XP_016866752.1:n.-154-5216G>A
NM_003449.5:c.-375-1589G>A MANE Select	NP_003440.1:n.-375-1589G>A
NM_001242783.2:c.-154-5216G>A	NP_001229712.1:n.-154-5216G>A