Canonical Allele Identifier: CA2466857763
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997000_154997001delinsCA , CM000685.2:g.154997000_154997001delinsCA GRCh38
NC_000023.10:g.154225275_154225276delinsCA , CM000685.1:g.154225275_154225276delinsCA GRCh37
NC_000023.9:g.153878469_153878470delinsCA NCBI36
NG_011403.1:g.30723_30724delinsTG
NG_011403.2:g.30723_30724delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.360_361delinsTG MANE Select ENSP00000353393.4:p.Val120=
ENST00000647125.1:c.*146_*147delinsTG ENSP00000496062.1:n.*146_*147delinsTG
ENST00000360256.8:c.360_361delinsTG ENSP00000353393.4:p.Val120=
ENST00000423959.5:c.255_256delinsTG ENSP00000409446.1:p.Val85=
ENST00000453950.1:c.342_343delinsTG ENSP00000389153.1:p.Val114=
NM_000132.3:c.360_361delinsTG NP_000123.1:p.Val120=
XM_011531126.1:c.255_256delinsTG XP_011529428.1:p.Val85=
NM_000132.4:c.360_361delinsTG MANE Select NP_000123.1:p.Val120=