Canonical Allele Identifier: CA2466845305
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956975_154956977delinsTAC , CM000685.2:g.154956975_154956977delinsTAC GRCh38
NC_000023.10:g.154185250_154185252delinsTAC , CM000685.1:g.154185250_154185252delinsTAC GRCh37
NC_000023.9:g.153838444_153838446delinsTAC NCBI36
NG_011403.1:g.70747_70749delinsGTA
NG_011403.2:g.70747_70749delinsGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1732_1734delinsGTA MANE Select ENSP00000353393.4:p.Val578=
ENST00000647125.1:c.*1608_*1610delinsGTA ENSP00000496062.1:n.*1608_*1610delinsGTA
ENST00000360256.8:c.1732_1734delinsGTA ENSP00000353393.4:p.Val578=
NM_000132.3:c.1732_1734delinsGTA NP_000123.1:p.Val578=
XM_011531126.1:c.1627_1629delinsGTA XP_011529428.1:p.Val543=
NM_000132.4:c.1732_1734delinsGTA MANE Select NP_000123.1:p.Val578=