Canonical Allele Identifier: CA2466807448
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837699_154837700delinsTG , CM000685.2:g.154837699_154837700delinsTG GRCh38
NC_000023.10:g.154065974_154065975delinsTG , CM000685.1:g.154065974_154065975delinsTG GRCh37
NC_000023.9:g.153719168_153719169delinsTG NCBI36
NG_011403.1:g.190024_190025delinsCA
NG_033065.1:g.1963_1964delinsCA
NG_011403.2:g.190024_190025delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6953_6954delinsCA MANE Select ENSP00000353393.4:p.Pro2318=
ENST00000644698.1:c.686_687delinsCA ENSP00000495706.1:p.Pro229=
ENST00000330287.10:c.548_549delinsCA ENSP00000327895.6:p.Pro183=
ENST00000360256.8:c.6953_6954delinsCA ENSP00000353393.4:p.Pro2318=
NM_000132.3:c.6953_6954delinsCA NP_000123.1:p.Pro2318=
NM_019863.2:c.548_549delinsCA NP_063916.1:p.Pro183=
XM_011531126.1:c.6848_6849delinsCA XP_011529428.1:p.Pro2283=
NM_000132.4:c.6953_6954delinsCA MANE Select NP_000123.1:p.Pro2318=
NM_019863.3:c.548_549delinsCA NP_063916.1:p.Pro183=