Canonical Allele Identifier: CA2518054659

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572441_169572442insAG , CM000663.2:g.169572441_169572442insAG	GRCh38
NC_000001.10:g.169541679_169541680insAG , CM000663.1:g.169541679_169541680insAG	GRCh37
NC_000001.9:g.167808303_167808304insAG	NCBI36
NG_011806.1:g.19090_19091insCT , LRG_553:g.19090_19091insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-99_251-98insCT MANE Select	ENSP00000356771.3:n.251-99_251-98insCT
ENST00000367796.3:c.251-99_251-98insCT	ENSP00000356770.3:n.251-99_251-98insCT
ENST00000367797.7:c.251-99_251-98insCT	ENSP00000356771.3:n.251-99_251-98insCT
NM_000130.4:c.251-99_251-98insCT , LRG_553t1:c.251-99_251-98insCT	NP_000121.2:n.251-99_251-98insCT
XM_017000660.2:c.-161-99_-161-98insCT	XP_016856149.1:n.-161-99_-161-98insCT
NM_000130.5:c.251-99_251-98insCT MANE Select	NP_000121.2:n.251-99_251-98insCT