Canonical Allele Identifier: CA1206149250

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555221_169555222delinsAT , CM000663.2:g.169555221_169555222delinsAT	GRCh38
NC_000001.10:g.169524459_169524460delinsAT , CM000663.1:g.169524459_169524460delinsAT	GRCh37
NC_000001.9:g.167791083_167791084delinsAT	NCBI36
NG_011806.1:g.36310_36311delinsAT , LRG_553:g.36310_36311delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1078_1079delinsAT MANE Select	ENSP00000356771.3:p.Ile360=
ENST00000367796.3:c.1078_1079delinsAT	ENSP00000356770.3:p.Ile360=
ENST00000367797.7:c.1078_1079delinsAT	ENSP00000356771.3:p.Ile360=
NM_000130.4:c.1078_1079delinsAT , LRG_553t1:c.1078_1079delinsAT	NP_000121.2:p.Ile360=
XM_017000660.2:c.667_668delinsAT	XP_016856149.1:p.Ile223=
NM_000130.5:c.1078_1079delinsAT MANE Select	NP_000121.2:p.Ile360=