Canonical Allele Identifier: CA1206146526

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552224_169552225delinsTG , CM000663.2:g.169552224_169552225delinsTG	GRCh38
NC_000001.10:g.169521462_169521463delinsTG , CM000663.1:g.169521462_169521463delinsTG	GRCh37
NC_000001.9:g.167788086_167788087delinsTG	NCBI36
NG_011806.1:g.39307_39308delinsCA , LRG_553:g.39307_39308delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1296+332_1296+333delinsCA MANE Select	ENSP00000356771.3:n.1296+332_1296+333delinsCA
ENST00000367796.3:c.1296+332_1296+333delinsCA	ENSP00000356770.3:n.1296+332_1296+333delinsCA
ENST00000367797.7:c.1296+332_1296+333delinsCA	ENSP00000356771.3:n.1296+332_1296+333delinsCA
NM_000130.4:c.1296+332_1296+333delinsCA , LRG_553t1:c.1296+332_1296+333delinsCA	NP_000121.2:n.1296+332_1296+333delinsCA
XM_017000660.2:c.885+332_885+333delinsCA	XP_016856149.1:n.885+332_885+333delinsCA
NM_000130.5:c.1296+332_1296+333delinsCA MANE Select	NP_000121.2:n.1296+332_1296+333delinsCA