Canonical Allele Identifier: CA1206148722

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572338G= , CM000663.2:g.169572338G=	GRCh38
NC_000001.10:g.169541576G= , CM000663.1:g.169541576G=	GRCh37
NC_000001.9:g.167808200G=	NCBI36
NG_011806.1:g.19194C= , LRG_553:g.19194C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.256C= MANE Select	ENSP00000356771.3:p.Leu86=
ENST00000367796.3:c.256C=	ENSP00000356770.3:p.Leu86=
ENST00000367797.7:c.256C=	ENSP00000356771.3:p.Leu86=
NM_000130.4:c.256C= , LRG_553t1:c.256C=	NP_000121.2:p.Leu86=
XM_017000660.2:c.-156C=	XP_016856149.1:n.-156C=
NM_000130.5:c.256C= MANE Select	NP_000121.2:p.Leu86=