Canonical Allele Identifier: CA1206144042

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549632_169549633delinsGA , CM000663.2:g.169549632_169549633delinsGA	GRCh38
NC_000001.10:g.169518870_169518871delinsGA , CM000663.1:g.169518870_169518871delinsGA	GRCh37
NC_000001.9:g.167785494_167785495delinsGA	NCBI36
NG_011806.1:g.41899_41900delinsTC , LRG_553:g.41899_41900delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1611+168_1611+169delinsTC MANE Select	ENSP00000356771.3:n.1611+168_1611+169delinsTC
ENST00000367796.3:c.1611+168_1611+169delinsTC	ENSP00000356770.3:n.1611+168_1611+169delinsTC
ENST00000367797.7:c.1611+168_1611+169delinsTC	ENSP00000356771.3:n.1611+168_1611+169delinsTC
NM_000130.4:c.1611+168_1611+169delinsTC , LRG_553t1:c.1611+168_1611+169delinsTC	NP_000121.2:n.1611+168_1611+169delinsTC
XM_017000660.2:c.1200+168_1200+169delinsTC	XP_016856149.1:n.1200+168_1200+169delinsTC
NM_000130.5:c.1611+168_1611+169delinsTC MANE Select	NP_000121.2:n.1611+168_1611+169delinsTC