Canonical Allele Identifier: CA1206140033

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541017G= , CM000663.2:g.169541017G=	GRCh38
NC_000001.10:g.169510255G= , CM000663.1:g.169510255G=	GRCh37
NC_000001.9:g.167776879G=	NCBI36
NG_011806.1:g.50515C= , LRG_553:g.50515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4073C= MANE Select	ENSP00000356771.3:p.Ser1358=
ENST00000367796.3:c.4088C=	ENSP00000356770.3:p.Ser1363=
ENST00000367797.7:c.4073C=	ENSP00000356771.3:p.Ser1358=
NM_000130.4:c.4073C= , LRG_553t1:c.4073C=	NP_000121.2:p.Ser1358=
XM_017000660.2:c.3662C=	XP_016856149.1:p.Ser1221=
NM_000130.5:c.4073C= MANE Select	NP_000121.2:p.Ser1358=