Canonical Allele Identifier: CA2401956132

Gene: BPIFC

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32413845T>G , CM000684.2:g.32413845T>G	GRCh38
NC_000022.10:g.32809832T>G , CM000684.1:g.32809832T>G	GRCh37
NC_000022.9:g.31139832T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300399.9:c.*458A>C MANE Select	ENSP00000300399.3:n.*458A>C
XM_011530088.1:c.*458A>C	XP_011528390.1:n.*458A>C
XM_011530089.1:c.*458A>C	XP_011528391.1:n.*458A>C
XM_011530090.1:c.*458A>C	XP_011528392.1:n.*458A>C
XM_011530091.1:c.*458A>C	XP_011528393.1:n.*458A>C
XM_011530092.1:c.*458A>C	XP_011528394.1:n.*458A>C
XM_011530093.1:c.*458A>C	XP_011528395.1:n.*458A>C
XM_011530088.2:c.*458A>C	XP_011528390.1:n.*458A>C
XM_011530089.2:c.*458A>C	XP_011528391.1:n.*458A>C
XM_011530090.2:c.*458A>C	XP_011528392.1:n.*458A>C
XM_011530091.2:c.*458A>C	XP_011528393.1:n.*458A>C
XM_017028740.1:c.*458A>C	XP_016884229.1:n.*458A>C
NM_174932.3:c.*458A>C MANE Select	NP_777592.1:n.*458A>C