Canonical Allele Identifier: CA2695238486
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997055_154997056insTAAGAACATAAATCTCAG , CM000685.2:g.154997055_154997056insTAAGAACATAAATCTCAG GRCh38
NC_000023.10:g.154225330_154225331insTAAGAACATAAATCTCAG , CM000685.1:g.154225330_154225331insTAAGAACATAAATCTCAG GRCh37
NC_000023.9:g.153878524_153878525insTAAGAACATAAATCTCAG NCBI36
NG_011403.1:g.30668_30669insCTGAGATTTATGTTCTTA
NG_011403.2:g.30668_30669insCTGAGATTTATGTTCTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.305_306insCTGAGATTTATGTTCTTA MANE Select ENSP00000353393.4:p.Thr103Ter
ENST00000647125.1:c.*91_*92insCTGAGATTTATGTTCTTA ENSP00000496062.1:n.*91_*92insCTGAGATTTATGTTCTTA
ENST00000360256.8:c.305_306insCTGAGATTTATGTTCTTA ENSP00000353393.4:p.Thr103Ter
ENST00000423959.5:c.200_201insCTGAGATTTATGTTCTTA ENSP00000409446.1:p.Thr68Ter
ENST00000453950.1:c.287_288insCTGAGATTTATGTTCTTA ENSP00000389153.1:p.Thr97Ter
NM_000132.3:c.305_306insCTGAGATTTATGTTCTTA NP_000123.1:p.Thr103Ter
XM_011531126.1:c.200_201insCTGAGATTTATGTTCTTA XP_011529428.1:p.Thr68Ter
NM_000132.4:c.305_306insCTGAGATTTATGTTCTTA MANE Select NP_000123.1:p.Thr103Ter