Canonical Allele Identifier: CA1206144023

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549625T= , CM000663.2:g.169549625T=	GRCh38
NC_000001.10:g.169518863T= , CM000663.1:g.169518863T=	GRCh37
NC_000001.9:g.167785487T=	NCBI36
NG_011806.1:g.41907A= , LRG_553:g.41907A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+176A= MANE Select	ENSP00000356771.3:n.1611+176A=
ENST00000367796.3:c.1611+176A=	ENSP00000356770.3:n.1611+176A=
ENST00000367797.7:c.1611+176A=	ENSP00000356771.3:n.1611+176A=
NM_000130.4:c.1611+176A= , LRG_553t1:c.1611+176A=	NP_000121.2:n.1611+176A=
XM_017000660.2:c.1200+176A=	XP_016856149.1:n.1200+176A=
NM_000130.5:c.1611+176A= MANE Select	NP_000121.2:n.1611+176A=