Canonical Allele Identifier: CA1206148737

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572353_169572354delinsCA , CM000663.2:g.169572353_169572354delinsCA	GRCh38
NC_000001.10:g.169541591_169541592delinsCA , CM000663.1:g.169541591_169541592delinsCA	GRCh37
NC_000001.9:g.167808215_167808216delinsCA	NCBI36
NG_011806.1:g.19178_19179delinsTG , LRG_553:g.19178_19179delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.251-11_251-10delinsTG MANE Select	ENSP00000356771.3:n.251-11_251-10delinsTG
ENST00000367796.3:c.251-11_251-10delinsTG	ENSP00000356770.3:n.251-11_251-10delinsTG
ENST00000367797.7:c.251-11_251-10delinsTG	ENSP00000356771.3:n.251-11_251-10delinsTG
NM_000130.4:c.251-11_251-10delinsTG , LRG_553t1:c.251-11_251-10delinsTG	NP_000121.2:n.251-11_251-10delinsTG
XM_017000660.2:c.-161-11_-161-10delinsTG	XP_016856149.1:n.-161-11_-161-10delinsTG
NM_000130.5:c.251-11_251-10delinsTG MANE Select	NP_000121.2:n.251-11_251-10delinsTG