Canonical Allele Identifier: CA1206148840

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572496T= , CM000663.2:g.169572496T=	GRCh38
NC_000001.10:g.169541734T= , CM000663.1:g.169541734T=	GRCh37
NC_000001.9:g.167808358T=	NCBI36
NG_011806.1:g.19036A= , LRG_553:g.19036A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-153A= MANE Select	ENSP00000356771.3:n.251-153A=
ENST00000367796.3:c.251-153A=	ENSP00000356770.3:n.251-153A=
ENST00000367797.7:c.251-153A=	ENSP00000356771.3:n.251-153A=
NM_000130.4:c.251-153A= , LRG_553t1:c.251-153A=	NP_000121.2:n.251-153A=
XM_017000660.2:c.-161-153A=	XP_016856149.1:n.-161-153A=
NM_000130.5:c.251-153A= MANE Select	NP_000121.2:n.251-153A=