Canonical Allele Identifier: CA2466807465

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837734_154837739delinsCTTGAT , CM000685.2:g.154837734_154837739delinsCTTGAT	GRCh38
NC_000023.10:g.154066009_154066014delinsCTTGAT , CM000685.1:g.154066009_154066014delinsCTTGAT	GRCh37
NC_000023.9:g.153719203_153719208delinsCTTGAT	NCBI36
NG_011403.1:g.189985_189990delinsATCAAG
NG_033065.1:g.1924_1929delinsATCAAG
NG_011403.2:g.189985_189990delinsATCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6914_6919delinsATCAAG MANE Select	ENSP00000353393.4:p.Asn2305=
ENST00000644698.1:c.647_652delinsATCAAG	ENSP00000495706.1:p.Asn216=
ENST00000330287.10:c.509_514delinsATCAAG	ENSP00000327895.6:p.Asn170=
ENST00000360256.8:c.6914_6919delinsATCAAG	ENSP00000353393.4:p.Asn2305=
NM_000132.3:c.6914_6919delinsATCAAG	NP_000123.1:p.Asn2305=
NM_019863.2:c.509_514delinsATCAAG	NP_063916.1:p.Asn170=
XM_011531126.1:c.6809_6814delinsATCAAG	XP_011529428.1:p.Asn2270=
NM_000132.4:c.6914_6919delinsATCAAG MANE Select	NP_000123.1:p.Asn2305=
NM_019863.3:c.509_514delinsATCAAG	NP_063916.1:p.Asn170=