Canonical Allele Identifier: CA2466807338
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837431_154837432delinsGC , CM000685.2:g.154837431_154837432delinsGC GRCh38
NC_000023.10:g.154065706_154065707delinsGC , CM000685.1:g.154065706_154065707delinsGC GRCh37
NC_000023.9:g.153718900_153718901delinsGC NCBI36
NG_011403.1:g.190292_190293delinsGC
NG_033065.1:g.2231_2232delinsGC
NG_011403.2:g.190292_190293delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*165_*166delinsGC MANE Select ENSP00000353393.4:n.*165_*166delinsGC
ENST00000644698.1:c.*165_*166delinsGC ENSP00000495706.1:n.*165_*166delinsGC
ENST00000330287.10:c.*165_*166delinsGC ENSP00000327895.6:n.*165_*166delinsGC
ENST00000360256.8:c.*165_*166delinsGC ENSP00000353393.4:n.*165_*166delinsGC
NM_000132.3:c.*165_*166delinsGC NP_000123.1:n.*165_*166delinsGC
NM_019863.2:c.*165_*166delinsGC NP_063916.1:n.*165_*166delinsGC
XM_011531126.1:c.*165_*166delinsGC XP_011529428.1:n.*165_*166delinsGC
NM_000132.4:c.*165_*166delinsGC MANE Select NP_000123.1:n.*165_*166delinsGC
NM_019863.3:c.*165_*166delinsGC NP_063916.1:n.*165_*166delinsGC