Canonical Allele Identifier: CA2746577457

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532363G>A , CM000663.2:g.169532363G>A	GRCh38
NC_000001.10:g.169501601G>A , CM000663.1:g.169501601G>A	GRCh37
NC_000001.9:g.167768225G>A	NCBI36
NG_011806.1:g.59169C>T , LRG_553:g.59169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1341C>T MANE Select	ENSP00000356771.3:n.4972-1341C>T
ENST00000367796.3:c.4987-1341C>T	ENSP00000356770.3:n.4987-1341C>T
ENST00000367797.7:c.4972-1341C>T	ENSP00000356771.3:n.4972-1341C>T
NM_000130.4:c.4972-1341C>T , LRG_553t1:c.4972-1341C>T	NP_000121.2:n.4972-1341C>T
XM_017000660.2:c.4561-1341C>T	XP_016856149.1:n.4561-1341C>T
NM_000130.5:c.4972-1341C>T MANE Select	NP_000121.2:n.4972-1341C>T