Canonical Allele Identifier: CA1206132329

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541668G= , CM000663.2:g.169541668G=	GRCh38
NC_000001.10:g.169510906G= , CM000663.1:g.169510906G=	GRCh37
NC_000001.9:g.167777530G=	NCBI36
NG_011806.1:g.49864C= , LRG_553:g.49864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3422C= MANE Select	ENSP00000356771.3:p.Thr1141=
ENST00000367796.3:c.3437C=	ENSP00000356770.3:p.Thr1146=
ENST00000367797.7:c.3422C=	ENSP00000356771.3:p.Thr1141=
NM_000130.4:c.3422C= , LRG_553t1:c.3422C=	NP_000121.2:p.Thr1141=
XM_017000660.2:c.3011C=	XP_016856149.1:p.Thr1004=
NM_000130.5:c.3422C= MANE Select	NP_000121.2:p.Thr1141=