Canonical Allele Identifier: CA1206148997

Gene: F5

Linked Data

• dbSNP Id: rs1660276054

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169554982_169554983insAT , CM000663.2:g.169554982_169554983insAT	GRCh38
NC_000001.10:g.169524220_169524221insAT , CM000663.1:g.169524220_169524221insAT	GRCh37
NC_000001.9:g.167790844_167790845insAT	NCBI36
NG_011806.1:g.36550_36551insTA , LRG_553:g.36550_36551insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+200_1118+201insTA MANE Select	ENSP00000356771.3:n.1118+200_1118+201insTA
ENST00000367796.3:c.1118+200_1118+201insTA	ENSP00000356770.3:n.1118+200_1118+201insTA
ENST00000367797.7:c.1118+200_1118+201insTA	ENSP00000356771.3:n.1118+200_1118+201insTA
NM_000130.4:c.1118+200_1118+201insTA , LRG_553t1:c.1118+200_1118+201insTA	NP_000121.2:n.1118+200_1118+201insTA
XM_017000660.2:c.707+200_707+201insTA	XP_016856149.1:n.707+200_707+201insTA
NM_000130.5:c.1118+200_1118+201insTA MANE Select	NP_000121.2:n.1118+200_1118+201insTA