Canonical Allele Identifier: CA343125043

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525972C>T , CM000663.2:g.169525972C>T	GRCh38
NC_000001.10:g.169495210C>T , CM000663.1:g.169495210C>T	GRCh37
NC_000001.9:g.167761834C>T	NCBI36
NG_011806.1:g.65560G>A , LRG_553:g.65560G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.5645G>A MANE Select	NP_000121.2:p.Trp1882Ter
ENST00000367797.9:c.5645G>A MANE Select	ENSP00000356771.3:p.Trp1882Ter
NM_000130.4:c.5645G>A , LRG_553t1:c.5645G>A	NP_000121.2:p.Trp1882Ter
ENST00000367796.3:c.5660G>A	ENSP00000356770.3:p.Trp1887Ter
ENST00000367797.7:c.5645G>A	ENSP00000356771.3:p.Trp1882Ter
XM_017000660.2:c.5234G>A	XP_016856149.1:p.Trp1745Ter