Canonical Allele Identifier: CA15424857
Gene: TRIM26 HGNC NCBI

Linked Data

dbSNP Id: rs2523722
gnomAD v2: 6-30165273-C-T
gnomAD v3: 6-30197496-C-T
gnomAD v4: 6-30197496-C-T
MyVariant Identifiers: chr6:g.30165273C>T (hg19) chr6:g.30197496C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30197496C>T , CM000668.2:g.30197496C>T GRCh38
NC_000006.11:g.30165273C>T , CM000668.1:g.30165273C>T GRCh37
NC_000006.10:g.30273252C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454678.7:c.535-750G>A MANE Select ENSP00000410446.2:n.535-750G>A
ENST00000416596.5:c.535-750G>A ENSP00000413673.1:n.535-750G>A
ENST00000437089.5:c.535-750G>A ENSP00000395491.1:n.535-750G>A
ENST00000453195.5:c.535-750G>A ENSP00000391879.1:n.535-750G>A
ENST00000454678.6:c.535-750G>A ENSP00000410446.2:n.535-750G>A
NM_001242783.1:c.535-750G>A NP_001229712.1:n.535-750G>A
NM_003449.4:c.535-750G>A NP_003440.1:n.535-750G>A
XM_005249374.2:c.535-750G>A XP_005249431.1:n.535-750G>A
XM_005249375.2:c.535-750G>A XP_005249432.1:n.535-750G>A
XM_005249376.2:c.535-750G>A XP_005249433.1:n.535-750G>A
XM_005249377.2:c.535-750G>A XP_005249434.1:n.535-750G>A
XM_005249378.2:c.535-750G>A XP_005249435.1:n.535-750G>A
XM_006715180.2:c.535-750G>A XP_006715243.1:n.535-750G>A
XM_011514859.1:c.534+933G>A XP_011513161.1:n.534+933G>A
XM_017011263.1:c.534+933G>A XP_016866752.1:n.534+933G>A
NM_003449.5:c.535-750G>A MANE Select NP_003440.1:n.535-750G>A
NM_001242783.2:c.535-750G>A NP_001229712.1:n.535-750G>A
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