Canonical Allele Identifier: CA1206147053

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552766_169552780delinsTTTCTCAAATAGAGA , CM000663.2:g.169552766_169552780delinsTTTCTCAAATAGAGA	GRCh38
NC_000001.10:g.169522004_169522018delinsTTTCTCAAATAGAGA , CM000663.1:g.169522004_169522018delinsTTTCTCAAATAGAGA	GRCh37
NC_000001.9:g.167788628_167788642delinsTTTCTCAAATAGAGA	NCBI36
NG_011806.1:g.38752_38766delinsTCTCTATTTGAGAAA , LRG_553:g.38752_38766delinsTCTCTATTTGAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1119-46_1119-32delinsTCTCTATTTGAGAAA MANE Select	ENSP00000356771.3:n.1119-46_1119-32delinsTCTCTATTTGAGAAA
ENST00000367796.3:c.1119-46_1119-32delinsTCTCTATTTGAGAAA	ENSP00000356770.3:n.1119-46_1119-32delinsTCTCTATTTGAGAAA
ENST00000367797.7:c.1119-46_1119-32delinsTCTCTATTTGAGAAA	ENSP00000356771.3:n.1119-46_1119-32delinsTCTCTATTTGAGAAA
NM_000130.4:c.1119-46_1119-32delinsTCTCTATTTGAGAAA , LRG_553t1:c.1119-46_1119-32delinsTCTCTATTTGAGAAA	NP_000121.2:n.1119-46_1119-32delinsTCTCTATTTGAGAAA
XM_017000660.2:c.708-46_708-32delinsTCTCTATTTGAGAAA	XP_016856149.1:n.708-46_708-32delinsTCTCTATTTGAGAAA
NM_000130.5:c.1119-46_1119-32delinsTCTCTATTTGAGAAA MANE Select	NP_000121.2:n.1119-46_1119-32delinsTCTCTATTTGAGAAA