Canonical Allele Identifier: CA1206149284

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555244G= , CM000663.2:g.169555244G=	GRCh38
NC_000001.10:g.169524482G= , CM000663.1:g.169524482G=	GRCh37
NC_000001.9:g.167791106G=	NCBI36
NG_011806.1:g.36288C= , LRG_553:g.36288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1056C= MANE Select	ENSP00000356771.3:p.Tyr352=
ENST00000367796.3:c.1056C=	ENSP00000356770.3:p.Tyr352=
ENST00000367797.7:c.1056C=	ENSP00000356771.3:p.Tyr352=
NM_000130.4:c.1056C= , LRG_553t1:c.1056C=	NP_000121.2:p.Tyr352=
XM_017000660.2:c.645C=	XP_016856149.1:p.Tyr215=
NM_000130.5:c.1056C= MANE Select	NP_000121.2:p.Tyr352=