Canonical Allele Identifier: CA1148899195

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541689T= , CM000663.2:g.169541689T=	GRCh38
NC_000001.10:g.169510927T= , CM000663.1:g.169510927T=	GRCh37
NC_000001.9:g.167777551T=	NCBI36
NG_011806.1:g.49843A= , LRG_553:g.49843A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3401A= MANE Select	ENSP00000356771.3:p.Asp1134=
ENST00000367796.3:c.3416A=	ENSP00000356770.3:p.Asp1139=
ENST00000367797.7:c.3401A=	ENSP00000356771.3:p.Asp1134=
NM_000130.4:c.3401A= , LRG_553t1:c.3401A=	NP_000121.2:p.Asp1134=
XM_017000660.2:c.2990A=	XP_016856149.1:p.Asp997=
NM_000130.5:c.3401A= MANE Select	NP_000121.2:p.Asp1134=