Canonical Allele Identifier: CA12279959
Gene: BCLAF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136288212C>T , CM000668.2:g.136288212C>T GRCh38
NC_000006.11:g.136609350C>T , CM000668.1:g.136609350C>T GRCh37
NC_000006.10:g.136651043C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000531224.6:c.-115+1501G>A MANE Select ENSP00000435210.1:n.-115+1501G>A
ENST00000640069.1:c.-115+1501G>A ENSP00000491530.1:n.-115+1501G>A
ENST00000353331.8:c.-115+1501G>A ENSP00000229446.5:n.-115+1501G>A
ENST00000527536.5:c.-115+1501G>A ENSP00000435441.1:n.-115+1501G>A
ENST00000527613.5:c.-115+1501G>A ENSP00000436216.1:n.-115+1501G>A
ENST00000527759.5:c.-115+1501G>A ENSP00000434826.1:n.-115+1501G>A
ENST00000528229.1:n.75+1501G>A
ENST00000529826.5:c.-115+1501G>A ENSP00000431734.1:n.-115+1501G>A
ENST00000530429.5:c.-115+1501G>A ENSP00000436142.1:n.-115+1501G>A
ENST00000530767.5:c.-115+1501G>A ENSP00000436501.1:n.-115+1501G>A
ENST00000531224.5:c.-115+1501G>A ENSP00000435210.1:n.-115+1501G>A
ENST00000532384.5:c.-115+1501G>A ENSP00000433505.1:n.-115+1501G>A
ENST00000534269.5:c.-115+1501G>A ENSP00000433822.1:n.-115+1501G>A
ENST00000628517.2:c.-115+1501G>A ENSP00000487249.1:n.-115+1501G>A
NM_001077440.1:c.-115+1501G>A NP_001070908.1:n.-115+1501G>A
NM_001077441.1:c.-115+1501G>A NP_001070909.1:n.-115+1501G>A
NM_001301038.1:c.-115+1501G>A NP_001287967.1:n.-115+1501G>A
NM_014739.2:c.-115+1501G>A NP_055554.1:n.-115+1501G>A
XM_005267237.2:c.-115+1501G>A XP_005267294.1:n.-115+1501G>A
XM_005267238.2:c.-115+1501G>A XP_005267295.1:n.-115+1501G>A
XR_245558.2:n.933+1501G>A
XR_245559.2:n.933+1501G>A
XR_942640.1:n.933+1501G>A
NM_001363659.1:c.-115+1501G>A NP_001350588.1:n.-115+1501G>A
XM_017011529.2:c.-115+1501G>A XP_016867018.1:n.-115+1501G>A
XM_017011530.2:c.-115+1501G>A XP_016867019.1:n.-115+1501G>A
XM_017011531.2:c.-115+1501G>A XP_016867020.1:n.-115+1501G>A
XM_017011532.2:c.-2175+1501G>A XP_016867021.1:n.-2175+1501G>A
XR_001743764.2:n.132+1501G>A
XR_001743766.2:n.75+1501G>A
XR_001743768.2:n.132+1501G>A
XR_001743769.2:n.132+1501G>A
XR_001743770.2:n.132+1501G>A
XR_001743771.1:n.75+1501G>A
XR_002956319.1:n.132+1501G>A
XR_245558.4:n.132+1501G>A
XR_245559.4:n.132+1501G>A
NM_001077441.2:c.-115+1501G>A NP_001070909.1:n.-115+1501G>A
NM_001301038.2:c.-115+1501G>A NP_001287967.1:n.-115+1501G>A
NM_001363659.2:c.-115+1501G>A NP_001350588.1:n.-115+1501G>A
NM_014739.3:c.-115+1501G>A MANE Select NP_055554.1:n.-115+1501G>A
NM_001077440.3:c.-115+1501G>A NP_001070908.1:n.-115+1501G>A
NM_001077441.3:c.-115+1501G>A NP_001070909.1:n.-115+1501G>A
NM_001301038.3:c.-115+1501G>A NP_001287967.1:n.-115+1501G>A
NM_001363659.3:c.-115+1501G>A NP_001350588.1:n.-115+1501G>A
NM_001386693.1:c.-115+1501G>A NP_001373622.1:n.-115+1501G>A
NM_001386694.1:c.-115+1501G>A NP_001373623.1:n.-115+1501G>A
NM_001386695.1:c.-115+1501G>A NP_001373624.1:n.-115+1501G>A
NM_001386696.1:c.-115+1501G>A NP_001373625.1:n.-115+1501G>A
NM_001386697.1:c.-115+1501G>A NP_001373626.1:n.-115+1501G>A
NM_001386698.1:c.-115+1501G>A NP_001373627.1:n.-115+1501G>A
NM_001386699.1:c.-115+1501G>A NP_001373628.1:n.-115+1501G>A
NM_001386700.1:c.-260+1501G>A NP_001373629.1:n.-260+1501G>A
NM_001386701.1:c.-135+1501G>A NP_001373630.1:n.-135+1501G>A
NM_001386702.1:c.-135+1501G>A NP_001373631.1:n.-135+1501G>A
NM_001386703.1:c.-135+1501G>A NP_001373632.1:n.-135+1501G>A
NM_001386704.1:c.-112+1501G>A NP_001373633.1:n.-112+1501G>A
NR_170164.1:n.134+1501G>A
NR_170165.1:n.134+1501G>A
NR_170166.1:n.134+1501G>A
NR_170167.1:n.134+1501G>A
NR_170168.1:n.134+1501G>A
NR_170169.1:n.134+1501G>A
NR_170170.1:n.134+1501G>A
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