Canonical Allele Identifier: CA2466815669

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863201_154863202delinsAG , CM000685.2:g.154863201_154863202delinsAG	GRCh38
NC_000023.10:g.154091476_154091477delinsAG , CM000685.1:g.154091476_154091477delinsAG	GRCh37
NC_000023.9:g.153744670_153744671delinsAG	NCBI36
NG_011403.1:g.164522_164523delinsCT
NG_011403.2:g.164522_164523delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6455_6456delinsCT MANE Select	ENSP00000353393.4:p.Ser2152=
ENST00000644698.1:c.188_189delinsCT	ENSP00000495706.1:p.Ser63=
ENST00000330287.10:c.50_51delinsCT	ENSP00000327895.6:p.Ser17=
ENST00000360256.8:c.6455_6456delinsCT	ENSP00000353393.4:p.Ser2152=
NM_000132.3:c.6455_6456delinsCT	NP_000123.1:p.Ser2152=
NM_019863.2:c.50_51delinsCT	NP_063916.1:p.Ser17=
XM_011531126.1:c.6350_6351delinsCT	XP_011529428.1:p.Ser2117=
NM_000132.4:c.6455_6456delinsCT MANE Select	NP_000123.1:p.Ser2152=
NM_019863.3:c.50_51delinsCT	NP_063916.1:p.Ser17=