Canonical Allele Identifier: CA1206132587

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541992T= , CM000663.2:g.169541992T=	GRCh38
NC_000001.10:g.169511230T= , CM000663.1:g.169511230T=	GRCh37
NC_000001.9:g.167777854T=	NCBI36
NG_011806.1:g.49540A= , LRG_553:g.49540A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3098A= MANE Select	ENSP00000356771.3:p.Lys1033=
ENST00000367796.3:c.3113A=	ENSP00000356770.3:p.Lys1038=
ENST00000367797.7:c.3098A=	ENSP00000356771.3:p.Lys1033=
NM_000130.4:c.3098A= , LRG_553t1:c.3098A=	NP_000121.2:p.Lys1033=
XM_017000660.2:c.2687A=	XP_016856149.1:p.Lys896=
NM_000130.5:c.3098A= MANE Select	NP_000121.2:p.Lys1033=