Canonical Allele Identifier: CA1143423797

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555241G= , CM000663.2:g.169555241G=	GRCh38
NC_000001.10:g.169524479G= , CM000663.1:g.169524479G=	GRCh37
NC_000001.9:g.167791103G=	NCBI36
NG_011806.1:g.36291C= , LRG_553:g.36291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1059C= MANE Select	ENSP00000356771.3:p.Phe353=
ENST00000367796.3:c.1059C=	ENSP00000356770.3:p.Phe353=
ENST00000367797.7:c.1059C=	ENSP00000356771.3:p.Phe353=
NM_000130.4:c.1059C= , LRG_553t1:c.1059C=	NP_000121.2:p.Phe353=
XM_017000660.2:c.648C=	XP_016856149.1:p.Phe216=
NM_000130.5:c.1059C= MANE Select	NP_000121.2:p.Phe353=