Canonical Allele Identifier: CA2580584286

Gene: IFI16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159035859A>C , CM000663.2:g.159035859A>C	GRCh38
NC_000001.10:g.159005649A>C , CM000663.1:g.159005649A>C	GRCh37
NC_000001.9:g.157272273A>C	NCBI36
NG_029141.1:g.30968A>C
NG_029141.2:g.40890A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001376587.1:c.1329+3168A>C MANE Select	NP_001363516.1:n.1329+3168A>C
ENST00000295809.12:c.1329+3168A>C MANE Select	ENSP00000295809.7:n.1329+3168A>C
NM_001206567.1:c.1161+3168A>C	NP_001193496.1:n.1161+3168A>C
NM_001206567.2:c.1161+3168A>C	NP_001193496.1:n.1161+3168A>C
NM_001364867.1:c.1329+3168A>C	NP_001351796.1:n.1329+3168A>C
NM_001364867.2:c.1329+3168A>C	NP_001351796.1:n.1329+3168A>C
NM_001376588.1:c.1329+3168A>C	NP_001363517.1:n.1329+3168A>C
NM_001376589.1:c.1329+3168A>C	NP_001363518.1:n.1329+3168A>C
NM_001376591.1:c.1329+3168A>C	NP_001363520.1:n.1329+3168A>C
NM_001376592.1:c.1329+3168A>C	NP_001363521.1:n.1329+3168A>C
NM_005531.2:c.1329+3168A>C	NP_005522.2:n.1329+3168A>C
NM_005531.3:c.1329+3168A>C	NP_005522.2:n.1329+3168A>C
ENST00000295809.11:c.1329+3168A>C	ENSP00000295809.7:n.1329+3168A>C
ENST00000340979.10:c.-130+3168A>C	ENSP00000342741.7:n.-130+3168A>C
ENST00000359709.7:c.1161+3168A>C	ENSP00000352740.3:n.1161+3168A>C
ENST00000368131.8:c.1329+3168A>C	ENSP00000357113.4:n.1329+3168A>C
ENST00000368132.7:c.1329+3168A>C	ENSP00000357114.3:n.1329+3168A>C
ENST00000448393.6:c.1329+3168A>C	ENSP00000404325.2:n.1329+3168A>C
ENST00000483916.2:n.1593+3168A>C
ENST00000493884.5:n.1593+3168A>C
ENST00000562225.1:n.188+3168A>C
XM_005245127.2:c.1341+3168A>C	XP_005245184.1:n.1341+3168A>C
XM_006711290.1:c.1341+3168A>C	XP_006711353.1:n.1341+3168A>C
XM_006711290.2:c.1341+3168A>C	XP_006711353.1:n.1341+3168A>C
XM_011509478.1:c.1341+3168A>C	XP_011507780.1:n.1341+3168A>C
XM_017001149.2:c.1341+3168A>C	XP_016856638.1:n.1341+3168A>C
XM_017001150.2:c.1341+3168A>C	XP_016856639.1:n.1341+3168A>C