Canonical Allele Identifier: CA1206135835

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529743T= , CM000663.2:g.169529743T=	GRCh38
NC_000001.10:g.169498981T= , CM000663.1:g.169498981T=	GRCh37
NC_000001.9:g.167765605T=	NCBI36
NG_011806.1:g.61789A= , LRG_553:g.61789A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5284A= MANE Select	ENSP00000356771.3:p.Met1762=
ENST00000367796.3:c.5299A=	ENSP00000356770.3:p.Met1767=
ENST00000367797.7:c.5284A=	ENSP00000356771.3:p.Met1762=
NM_000130.4:c.5284A= , LRG_553t1:c.5284A=	NP_000121.2:p.Met1762=
XM_017000660.2:c.4873A=	XP_016856149.1:p.Met1625=
NM_000130.5:c.5284A= MANE Select	NP_000121.2:p.Met1762=