Canonical Allele Identifier: CA2694839892

Gene: F9

Linked Data

• gnomAD v4: X-139561835-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561835_139561836insT , CM000685.2:g.139561835_139561836insT	GRCh38
NC_000023.10:g.138643994_138643995insT , CM000685.1:g.138643994_138643995insT	GRCh37
NC_000023.9:g.138471660_138471661insT	NCBI36
NG_007994.1:g.36100_36101insT , LRG_556:g.36100_36101insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1150_1151insT MANE Select	ENSP00000218099.2:p.Arg384LeufsTer9
ENST00000643157.1:n.1723+94_1723+95insT
ENST00000218099.6:c.1150_1151insT	ENSP00000218099.2:p.Arg384LeufsTer9
ENST00000394090.2:c.1036_1037insT	ENSP00000377650.2:p.Arg346LeufsTer9
NM_000133.3:c.1150_1151insT , LRG_556t1:c.1150_1151insT	NP_000124.1:p.Arg384LeufsTer9
NM_001313913.1:c.1036_1037insT	NP_001300842.1:p.Arg346LeufsTer9
XM_005262397.3:c.1021_1022insT	XP_005262454.1:p.Arg341LeufsTer9
XM_005262397.4:c.1021_1022insT	XP_005262454.1:p.Arg341LeufsTer9
NM_000133.4:c.1150_1151insT MANE Select	NP_000124.1:p.Arg384LeufsTer9
NM_001313913.2:c.1036_1037insT	NP_001300842.1:p.Arg346LeufsTer9