Canonical Allele Identifier: CA2573948911

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552787del , CM000663.2:g.169552787del	GRCh38
NC_000001.10:g.169522025del , CM000663.1:g.169522025del	GRCh37
NC_000001.9:g.167788649del	NCBI36
NG_011806.1:g.38745del , LRG_553:g.38745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1119-53del MANE Select	ENSP00000356771.3:n.1119-53del
ENST00000367796.3:c.1119-53del	ENSP00000356770.3:n.1119-53del
ENST00000367797.7:c.1119-53del	ENSP00000356771.3:n.1119-53del
NM_000130.4:c.1119-53del , LRG_553t1:c.1119-53del	NP_000121.2:n.1119-53del
XM_017000660.2:c.708-53del	XP_016856149.1:n.708-53del
NM_000130.5:c.1119-53del MANE Select	NP_000121.2:n.1119-53del