Canonical Allele Identifier: CA32426122

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169523014_169523017del , CM000663.2:g.169523014_169523017del	GRCh38
NC_000001.10:g.169492252_169492255del , CM000663.1:g.169492252_169492255del	GRCh37
NC_000001.9:g.167758876_167758879del	NCBI36
NG_011806.1:g.68516_68519del , LRG_553:g.68516_68519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.6048+181_6048+184del MANE Select	ENSP00000356771.3:n.6048+181_6048+184del
ENST00000367796.3:c.6063+181_6063+184del	ENSP00000356770.3:n.6063+181_6063+184del
ENST00000367797.7:c.6048+181_6048+184del	ENSP00000356771.3:n.6048+181_6048+184del
NM_000130.4:c.6048+181_6048+184del , LRG_553t1:c.6048+181_6048+184del	NP_000121.2:n.6048+181_6048+184del
XM_017000660.2:c.5637+181_5637+184del	XP_016856149.1:n.5637+181_5637+184del
NM_000130.5:c.6048+181_6048+184del MANE Select	NP_000121.2:n.6048+181_6048+184del