Canonical Allele Identifier: CA1143700512

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555296T= , CM000663.2:g.169555296T=	GRCh38
NC_000001.10:g.169524534T= , CM000663.1:g.169524534T=	GRCh37
NC_000001.9:g.167791158T=	NCBI36
NG_011806.1:g.36236A= , LRG_553:g.36236A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1004A= MANE Select	ENSP00000356771.3:p.Asn335=
ENST00000367796.3:c.1004A=	ENSP00000356770.3:p.Asn335=
ENST00000367797.7:c.1004A=	ENSP00000356771.3:p.Asn335=
NM_000130.4:c.1004A= , LRG_553t1:c.1004A=	NP_000121.2:p.Asn335=
XM_017000660.2:c.593A=	XP_016856149.1:p.Asn198=
NM_000130.5:c.1004A= MANE Select	NP_000121.2:p.Asn335=