Canonical Allele Identifier: CA2573949032

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552825del , CM000663.2:g.169552825del	GRCh38
NC_000001.10:g.169522063del , CM000663.1:g.169522063del	GRCh37
NC_000001.9:g.167788687del	NCBI36
NG_011806.1:g.38708del , LRG_553:g.38708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1119-90del MANE Select	ENSP00000356771.3:n.1119-90del
ENST00000367796.3:c.1119-90del	ENSP00000356770.3:n.1119-90del
ENST00000367797.7:c.1119-90del	ENSP00000356771.3:n.1119-90del
NM_000130.4:c.1119-90del , LRG_553t1:c.1119-90del	NP_000121.2:n.1119-90del
XM_017000660.2:c.708-90del	XP_016856149.1:n.708-90del
NM_000130.5:c.1119-90del MANE Select	NP_000121.2:n.1119-90del