Canonical Allele Identifier: CA1206149012

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169554992_169554993delinsAT , CM000663.2:g.169554992_169554993delinsAT	GRCh38
NC_000001.10:g.169524230_169524231delinsAT , CM000663.1:g.169524230_169524231delinsAT	GRCh37
NC_000001.9:g.167790854_167790855delinsAT	NCBI36
NG_011806.1:g.36539_36540delinsAT , LRG_553:g.36539_36540delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+189_1118+190delinsAT MANE Select	ENSP00000356771.3:n.1118+189_1118+190delinsAT
ENST00000367796.3:c.1118+189_1118+190delinsAT	ENSP00000356770.3:n.1118+189_1118+190delinsAT
ENST00000367797.7:c.1118+189_1118+190delinsAT	ENSP00000356771.3:n.1118+189_1118+190delinsAT
NM_000130.4:c.1118+189_1118+190delinsAT , LRG_553t1:c.1118+189_1118+190delinsAT	NP_000121.2:n.1118+189_1118+190delinsAT
XM_017000660.2:c.707+189_707+190delinsAT	XP_016856149.1:n.707+189_707+190delinsAT
NM_000130.5:c.1118+189_1118+190delinsAT MANE Select	NP_000121.2:n.1118+189_1118+190delinsAT