Canonical Allele Identifier: CA2101551256
Gene: PIBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.72835266A= , CM000675.2:g.72835266A= GRCh38
NC_000013.10:g.73409404A= , CM000675.1:g.73409404A= GRCh37
NC_000013.9:g.72307405A= NCBI36
NG_053118.1:g.58243A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326291.11:c.1121A= MANE Select ENSP00000317144.6:p.Glu374=
ENST00000326291.10:c.1121A= ENSP00000317144.6:p.Glu374=
ENST00000492803.1:n.385A=
ENST00000615625.1:c.-238A= ENSP00000483286.1:n.-238A=
ENST00000617689.4:c.1121A= ENSP00000478697.1:p.Glu374=
NM_006346.2:c.1121A= NP_006337.2:p.Glu374=
XM_006719755.2:c.1144A= XP_006719818.1:p.Lys382=
XM_011534881.1:c.1121A= XP_011533183.1:p.Glu374=
XM_011534882.1:c.1121A= XP_011533184.1:p.Glu374=
XM_011534883.1:c.1121A= XP_011533185.1:p.Glu374=
XM_011534884.1:c.1121A= XP_011533186.1:p.Glu374=
XM_011534885.1:c.752A= XP_011533187.1:p.Glu251=
XM_011534886.1:c.1121A= XP_011533188.1:p.Glu374=
XR_941461.1:n.1271A=
NM_001349655.1:c.1121A= NP_001336584.1:p.Glu374=
NM_006346.3:c.1121A= NP_006337.2:p.Glu374=
NR_146205.1:n.1518A=
NR_146206.1:n.1518A=
XM_011534882.3:c.1121A= XP_011533184.1:p.Glu374=
XM_011534884.3:c.1121A= XP_011533186.1:p.Glu374=
XM_011534885.3:c.752A= XP_011533187.1:p.Glu251=
XM_011534886.3:c.1121A= XP_011533188.1:p.Glu374=
XM_017020350.2:c.752A= XP_016875839.1:p.Glu251=
XM_017020351.2:c.1121A= XP_016875840.1:p.Glu374=
XM_017020352.2:c.-83A= XP_016875841.1:n.-83A=
XM_017020354.2:c.-83A= XP_016875843.1:n.-83A=
XM_024449314.1:c.1121A= XP_024305082.1:p.Glu374=
XR_001749456.2:n.1385A=
XR_001749457.2:n.1385A=
XR_001749458.2:n.1385A=
XR_001749459.2:n.1385A=
XR_001749460.2:n.1385A=
XR_002957449.1:n.1385A=
XR_941461.3:n.1385A=
NM_006346.4:c.1121A= MANE Select NP_006337.2:p.Glu374=
NM_001349655.2:c.1121A= NP_001336584.1:p.Glu374=
NR_146205.2:n.1408A=
NR_146206.2:n.1408A=