Canonical Allele Identifier: CA7325187

Gene: IFI27L1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94096847T>C , CM000676.2:g.94096847T>C	GRCh38
NC_000014.8:g.94563193T>C , CM000676.1:g.94563193T>C	GRCh37
NC_000014.7:g.93632946T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_206949.3:c.-51-40T>C MANE Select	NP_996832.1:n.-51-40T>C
ENST00000555523.6:c.-51-40T>C MANE Select	ENSP00000451851.1:n.-51-40T>C
NM_145249.2:c.-91T>C	NP_660292.1:n.-91T>C
NM_145249.3:c.-91T>C	NP_660292.1:n.-91T>C
NM_206949.2:c.-51-40T>C	NP_996832.1:n.-51-40T>C
ENST00000393115.7:c.-91T>C	ENSP00000376824.3:n.-91T>C
ENST00000553350.5:n.150-40T>C
ENST00000553664.1:c.17-40T>C	ENSP00000451043.1:n.17-40T>C
ENST00000554166.5:c.-241-40T>C	ENSP00000452226.1:n.-241-40T>C
ENST00000554544.5:c.-82-9T>C	ENSP00000451676.1:n.-82-9T>C
ENST00000555341.5:c.-269-9T>C	ENSP00000451608.1:n.-269-9T>C
ENST00000555523.5:c.-51-40T>C	ENSP00000451851.1:n.-51-40T>C
ENST00000556381.5:c.-241-40T>C	ENSP00000451459.1:n.-241-40T>C
ENST00000557066.5:c.-82-9T>C	ENSP00000451889.1:n.-82-9T>C
ENST00000557218.5:c.-51-40T>C	ENSP00000450463.1:n.-51-40T>C
ENST00000557600.5:n.140-40T>C
XM_011536405.1:c.-82-9T>C	XP_011534707.1:n.-82-9T>C
XM_011536405.3:c.-82-9T>C	XP_011534707.1:n.-82-9T>C
XM_011536406.1:c.-269-9T>C	XP_011534708.1:n.-269-9T>C
XM_011536406.2:c.-269-9T>C	XP_011534708.1:n.-269-9T>C
XM_011536407.1:c.-272-9T>C	XP_011534709.1:n.-272-9T>C
XM_011536407.2:c.-272-9T>C	XP_011534709.1:n.-272-9T>C
XM_017020961.1:c.10-40T>C	XP_016876450.1:n.10-40T>C
XM_017020962.2:c.10-40T>C	XP_016876451.1:n.10-40T>C
XM_017020963.2:c.10-40T>C	XP_016876452.1:n.10-40T>C