Canonical Allele Identifier: CA1206140037

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541023G= , CM000663.2:g.169541023G=	GRCh38
NC_000001.10:g.169510261G= , CM000663.1:g.169510261G=	GRCh37
NC_000001.9:g.167776885G=	NCBI36
NG_011806.1:g.50509C= , LRG_553:g.50509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4067C= MANE Select	ENSP00000356771.3:p.Pro1356=
ENST00000367796.3:c.4082C=	ENSP00000356770.3:p.Pro1361=
ENST00000367797.7:c.4067C=	ENSP00000356771.3:p.Pro1356=
NM_000130.4:c.4067C= , LRG_553t1:c.4067C=	NP_000121.2:p.Pro1356=
XM_017000660.2:c.3656C=	XP_016856149.1:p.Pro1219=
NM_000130.5:c.4067C= MANE Select	NP_000121.2:p.Pro1356=