Canonical Allele Identifier: CA1206148648

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572283T= , CM000663.2:g.169572283T=	GRCh38
NC_000001.10:g.169541521T= , CM000663.1:g.169541521T=	GRCh37
NC_000001.9:g.167808145T=	NCBI36
NG_011806.1:g.19249A= , LRG_553:g.19249A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.311A= MANE Select	ENSP00000356771.3:p.Asn104=
ENST00000367796.3:c.311A=	ENSP00000356770.3:p.Asn104=
ENST00000367797.7:c.311A=	ENSP00000356771.3:p.Asn104=
NM_000130.4:c.311A= , LRG_553t1:c.311A=	NP_000121.2:p.Asn104=
XM_017000660.2:c.-101A=	XP_016856149.1:n.-101A=
NM_000130.5:c.311A= MANE Select	NP_000121.2:p.Asn104=