Canonical Allele Identifier: CA2466857760
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996995_154996997delinsTAC , CM000685.2:g.154996995_154996997delinsTAC GRCh38
NC_000023.10:g.154225270_154225272delinsTAC , CM000685.1:g.154225270_154225272delinsTAC GRCh37
NC_000023.9:g.153878464_153878466delinsTAC NCBI36
NG_011403.1:g.30727_30729delinsGTA
NG_011403.2:g.30727_30729delinsGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.364_366delinsGTA MANE Select ENSP00000353393.4:p.Val122=
ENST00000647125.1:c.*150_*152delinsGTA ENSP00000496062.1:n.*150_*152delinsGTA
ENST00000360256.8:c.364_366delinsGTA ENSP00000353393.4:p.Val122=
ENST00000423959.5:c.259_261delinsGTA ENSP00000409446.1:p.Val87=
ENST00000453950.1:c.346_348delinsGTA ENSP00000389153.1:p.Val116=
NM_000132.3:c.364_366delinsGTA NP_000123.1:p.Val122=
XM_011531126.1:c.259_261delinsGTA XP_011529428.1:p.Val87=
NM_000132.4:c.364_366delinsGTA MANE Select NP_000123.1:p.Val122=