Canonical Allele Identifier: CA2466807385

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837540_154837541delinsGC , CM000685.2:g.154837540_154837541delinsGC	GRCh38
NC_000023.10:g.154065815_154065816delinsGC , CM000685.1:g.154065815_154065816delinsGC	GRCh37
NC_000023.9:g.153719009_153719010delinsGC	NCBI36
NG_011403.1:g.190183_190184delinsGC
NG_033065.1:g.2122_2123delinsGC
NG_011403.2:g.190183_190184delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*56_*57delinsGC MANE Select	ENSP00000353393.4:n.*56_*57delinsGC
ENST00000644698.1:c.*56_*57delinsGC	ENSP00000495706.1:n.*56_*57delinsGC
ENST00000330287.10:c.*56_*57delinsGC	ENSP00000327895.6:n.*56_*57delinsGC
ENST00000360256.8:c.*56_*57delinsGC	ENSP00000353393.4:n.*56_*57delinsGC
NM_000132.3:c.*56_*57delinsGC	NP_000123.1:n.*56_*57delinsGC
NM_019863.2:c.*56_*57delinsGC	NP_063916.1:n.*56_*57delinsGC
XM_011531126.1:c.*56_*57delinsGC	XP_011529428.1:n.*56_*57delinsGC
NM_000132.4:c.*56_*57delinsGC MANE Select	NP_000123.1:n.*56_*57delinsGC
NM_019863.3:c.*56_*57delinsGC	NP_063916.1:n.*56_*57delinsGC