Canonical Allele Identifier: CA2466856533

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993043G= , CM000685.2:g.154993043G=	GRCh38
NC_000023.10:g.154221318G= , CM000685.1:g.154221318G=	GRCh37
NC_000023.9:g.153874512G=	NCBI36
NG_011403.1:g.34681C=
NG_011403.2:g.34681C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.494C= MANE Select	ENSP00000353393.4:p.Pro165=
ENST00000647125.1:c.*280C=	ENSP00000496062.1:n.*280C=
ENST00000360256.8:c.494C=	ENSP00000353393.4:p.Pro165=
ENST00000423959.5:c.389C=	ENSP00000409446.1:p.Pro130=
ENST00000453950.1:c.476C=	ENSP00000389153.1:p.Pro159=
NM_000132.3:c.494C=	NP_000123.1:p.Pro165=
XM_011531126.1:c.389C=	XP_011529428.1:p.Pro130=
NM_000132.4:c.494C= MANE Select	NP_000123.1:p.Pro165=