Canonical Allele Identifier: CA408870095
Community Standard Title: NM_001725.3(BPI):c.634G>C (p.Glu212Gln)
Gene: BPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38318446G>C , CM000682.2:g.38318446G>C GRCh38
NC_000020.10:g.36946848G>C , CM000682.1:g.36946848G>C GRCh37
NC_000020.9:g.36380262G>C NCBI36
NG_047016.1:g.19297G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001725.3:c.634G>C MANE Select NP_001716.3:p.Glu212Gln
ENST00000642449.2:c.634G>C MANE Select ENSP00000494528.2:p.Glu212Gln
NM_001725.2:c.646G>C NP_001716.2:p.Glu216Gln
ENST00000262865.8:c.646G>C ENSP00000262865.4:p.Glu216Gln
ENST00000262865.9:c.646G>C ENSP00000262865.4:p.Glu216Gln
ENST00000417318.3:c.43G>C ENSP00000409833.2:p.Glu15Gln
ENST00000489102.2:c.43G>C ENSP00000486976.1:p.Glu15Gln
XM_005260522.2:c.646G>C XP_005260579.1:p.Glu216Gln
XM_011529012.1:c.43G>C XP_011527314.1:p.Glu15Gln
XM_024451972.1:c.52G>C XP_024307740.1:p.Glu18Gln
XR_430313.2:n.675G>C