Canonical Allele Identifier: CA1206146957

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552713C= , CM000663.2:g.169552713C=	GRCh38
NC_000001.10:g.169521951C= , CM000663.1:g.169521951C=	GRCh37
NC_000001.9:g.167788575C=	NCBI36
NG_011806.1:g.38819G= , LRG_553:g.38819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1140G= MANE Select	ENSP00000356771.3:p.Leu380=
ENST00000367796.3:c.1140G=	ENSP00000356770.3:p.Leu380=
ENST00000367797.7:c.1140G=	ENSP00000356771.3:p.Leu380=
NM_000130.4:c.1140G= , LRG_553t1:c.1140G=	NP_000121.2:p.Leu380=
XM_017000660.2:c.729G=	XP_016856149.1:p.Leu243=
NM_000130.5:c.1140G= MANE Select	NP_000121.2:p.Leu380=