Canonical Allele Identifier: CA2746577907

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552394_169552397del , CM000663.2:g.169552394_169552397del	GRCh38
NC_000001.10:g.169521632_169521635del , CM000663.1:g.169521632_169521635del	GRCh37
NC_000001.9:g.167788256_167788259del	NCBI36
NG_011806.1:g.39136_39139del , LRG_553:g.39136_39139del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1296+161_1296+164del MANE Select	ENSP00000356771.3:n.1296+161_1296+164del
ENST00000367796.3:c.1296+161_1296+164del	ENSP00000356770.3:n.1296+161_1296+164del
ENST00000367797.7:c.1296+161_1296+164del	ENSP00000356771.3:n.1296+161_1296+164del
NM_000130.4:c.1296+161_1296+164del , LRG_553t1:c.1296+161_1296+164del	NP_000121.2:n.1296+161_1296+164del
XM_017000660.2:c.885+161_885+164del	XP_016856149.1:n.885+161_885+164del
NM_000130.5:c.1296+161_1296+164del MANE Select	NP_000121.2:n.1296+161_1296+164del