Canonical Allele Identifier: CA1143253988

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529822G= , CM000663.2:g.169529822G=	GRCh38
NC_000001.10:g.169499060G= , CM000663.1:g.169499060G=	GRCh37
NC_000001.9:g.167765684G=	NCBI36
NG_011806.1:g.61710C= , LRG_553:g.61710C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5209-4C= MANE Select	ENSP00000356771.3:n.5209-4C=
ENST00000367796.3:c.5224-4C=	ENSP00000356770.3:n.5224-4C=
ENST00000367797.7:c.5209-4C=	ENSP00000356771.3:n.5209-4C=
NM_000130.4:c.5209-4C= , LRG_553t1:c.5209-4C=	NP_000121.2:n.5209-4C=
XM_017000660.2:c.4798-4C=	XP_016856149.1:n.4798-4C=
NM_000130.5:c.5209-4C= MANE Select	NP_000121.2:n.5209-4C=