Canonical Allele Identifier: CA1206132475

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541831G= , CM000663.2:g.169541831G=	GRCh38
NC_000001.10:g.169511069G= , CM000663.1:g.169511069G=	GRCh37
NC_000001.9:g.167777693G=	NCBI36
NG_011806.1:g.49701C= , LRG_553:g.49701C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3259C= MANE Select	ENSP00000356771.3:p.Pro1087=
ENST00000367796.3:c.3274C=	ENSP00000356770.3:p.Pro1092=
ENST00000367797.7:c.3259C=	ENSP00000356771.3:p.Pro1087=
NM_000130.4:c.3259C= , LRG_553t1:c.3259C=	NP_000121.2:p.Pro1087=
XM_017000660.2:c.2848C=	XP_016856149.1:p.Pro950=
NM_000130.5:c.3259C= MANE Select	NP_000121.2:p.Pro1087=