Canonical Allele Identifier: CA9852409
Community Standard Title: NM_001725.3(BPI):c.1075G>A (p.Gly359Ser)
Gene: BPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38326346G>A , CM000682.2:g.38326346G>A GRCh38
NC_000020.10:g.36954748G>A , CM000682.1:g.36954748G>A GRCh37
NC_000020.9:g.36388162G>A NCBI36
NG_047016.1:g.27197G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001725.3:c.1075G>A MANE Select NP_001716.3:p.Gly359Ser
ENST00000642449.2:c.1075G>A MANE Select ENSP00000494528.2:p.Gly359Ser
NM_001725.2:c.1087G>A NP_001716.2:p.Gly363Ser
ENST00000262865.8:c.1087G>A ENSP00000262865.4:p.Gly363Ser
ENST00000262865.9:c.1087G>A ENSP00000262865.4:p.Gly363Ser
ENST00000417318.3:c.484G>A ENSP00000409833.2:p.Gly162Ser
ENST00000489102.2:c.*264G>A ENSP00000486976.1:n.*264G>A
XM_005260522.2:c.1087G>A XP_005260579.1:p.Gly363Ser
XM_011529012.1:c.484G>A XP_011527314.1:p.Gly162Ser
XM_024451972.1:c.493G>A XP_024307740.1:p.Gly165Ser
XR_430313.2:n.1116G>A