Canonical Allele Identifier: CA1206136796

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169532485_169532489delinsACTTC , CM000663.2:g.169532485_169532489delinsACTTC	GRCh38
NC_000001.10:g.169501723_169501727delinsACTTC , CM000663.1:g.169501723_169501727delinsACTTC	GRCh37
NC_000001.9:g.167768347_167768351delinsACTTC	NCBI36
NG_011806.1:g.59043_59047delinsGAAGT , LRG_553:g.59043_59047delinsGAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.4972-1467_4972-1463delinsGAAGT MANE Select	ENSP00000356771.3:n.4972-1467_4972-1463delinsGAAGT
ENST00000367796.3:c.4987-1467_4987-1463delinsGAAGT	ENSP00000356770.3:n.4987-1467_4987-1463delinsGAAGT
ENST00000367797.7:c.4972-1467_4972-1463delinsGAAGT	ENSP00000356771.3:n.4972-1467_4972-1463delinsGAAGT
NM_000130.4:c.4972-1467_4972-1463delinsGAAGT , LRG_553t1:c.4972-1467_4972-1463delinsGAAGT	NP_000121.2:n.4972-1467_4972-1463delinsGAAGT
XM_017000660.2:c.4561-1467_4561-1463delinsGAAGT	XP_016856149.1:n.4561-1467_4561-1463delinsGAAGT
NM_000130.5:c.4972-1467_4972-1463delinsGAAGT MANE Select	NP_000121.2:n.4972-1467_4972-1463delinsGAAGT