Canonical Allele Identifier: CA1206135860

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529828_169529830delinsCAG , CM000663.2:g.169529828_169529830delinsCAG	GRCh38
NC_000001.10:g.169499066_169499068delinsCAG , CM000663.1:g.169499066_169499068delinsCAG	GRCh37
NC_000001.9:g.167765690_167765692delinsCAG	NCBI36
NG_011806.1:g.61702_61704delinsCTG , LRG_553:g.61702_61704delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5209-12_5209-10delinsCTG MANE Select	ENSP00000356771.3:n.5209-12_5209-10delinsCTG
ENST00000367796.3:c.5224-12_5224-10delinsCTG	ENSP00000356770.3:n.5224-12_5224-10delinsCTG
ENST00000367797.7:c.5209-12_5209-10delinsCTG	ENSP00000356771.3:n.5209-12_5209-10delinsCTG
NM_000130.4:c.5209-12_5209-10delinsCTG , LRG_553t1:c.5209-12_5209-10delinsCTG	NP_000121.2:n.5209-12_5209-10delinsCTG
XM_017000660.2:c.4798-12_4798-10delinsCTG	XP_016856149.1:n.4798-12_4798-10delinsCTG
NM_000130.5:c.5209-12_5209-10delinsCTG MANE Select	NP_000121.2:n.5209-12_5209-10delinsCTG