Canonical Allele Identifier: CA14958380
Gene: BPIFC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32436887C>T , CM000684.2:g.32436887C>T GRCh38
NC_000022.10:g.32832874C>T , CM000684.1:g.32832874C>T GRCh37
NC_000022.9:g.31162874C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300399.9:c.747+873G>A MANE Select ENSP00000300399.3:n.747+873G>A
ENST00000534972.4:c.833+873G>A ENSP00000439123.3:n.833+873G>A
ENST00000300399.7:c.747+873G>A ENSP00000300399.3:n.747+873G>A
ENST00000397452.5:c.747+873G>A ENSP00000380594.1:n.747+873G>A
ENST00000534972.3:c.189+873G>A ENSP00000439123.2:n.189+873G>A
NM_174932.2:c.747+873G>A NP_777592.1:n.747+873G>A
XM_011530088.1:c.747+873G>A XP_011528390.1:n.747+873G>A
XM_011530089.1:c.747+873G>A XP_011528391.1:n.747+873G>A
XM_011530090.1:c.747+873G>A XP_011528392.1:n.747+873G>A
XM_011530091.1:c.591+873G>A XP_011528393.1:n.591+873G>A
XM_011530092.1:c.189+873G>A XP_011528394.1:n.189+873G>A
XM_011530093.1:c.189+873G>A XP_011528395.1:n.189+873G>A
XM_011530088.2:c.747+873G>A XP_011528390.1:n.747+873G>A
XM_011530089.2:c.747+873G>A XP_011528391.1:n.747+873G>A
XM_011530090.2:c.747+873G>A XP_011528392.1:n.747+873G>A
XM_011530091.2:c.591+873G>A XP_011528393.1:n.591+873G>A
XM_017028740.1:c.747+873G>A XP_016884229.1:n.747+873G>A
NM_174932.3:c.747+873G>A MANE Select NP_777592.1:n.747+873G>A
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