Canonical Allele Identifier: CA2466807462

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837727_154837730delinsAAGG , CM000685.2:g.154837727_154837730delinsAAGG	GRCh38
NC_000023.10:g.154066002_154066005delinsAAGG , CM000685.1:g.154066002_154066005delinsAAGG	GRCh37
NC_000023.9:g.153719196_153719199delinsAAGG	NCBI36
NG_011403.1:g.189994_189997delinsCCTT
NG_033065.1:g.1933_1936delinsCCTT
NG_011403.2:g.189994_189997delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6923_6926delinsCCTT MANE Select	ENSP00000353393.4:p.Ser2308=
ENST00000644698.1:c.656_659delinsCCTT	ENSP00000495706.1:p.Ser219=
ENST00000330287.10:c.518_521delinsCCTT	ENSP00000327895.6:p.Ser173=
ENST00000360256.8:c.6923_6926delinsCCTT	ENSP00000353393.4:p.Ser2308=
NM_000132.3:c.6923_6926delinsCCTT	NP_000123.1:p.Ser2308=
NM_019863.2:c.518_521delinsCCTT	NP_063916.1:p.Ser173=
XM_011531126.1:c.6818_6821delinsCCTT	XP_011529428.1:p.Ser2273=
NM_000132.4:c.6923_6926delinsCCTT MANE Select	NP_000123.1:p.Ser2308=
NM_019863.3:c.518_521delinsCCTT	NP_063916.1:p.Ser173=