Canonical Allele Identifier: CA2461412126

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561670_139561672delinsAGC , CM000685.2:g.139561670_139561672delinsAGC	GRCh38
NC_000023.10:g.138643829_138643831delinsAGC , CM000685.1:g.138643829_138643831delinsAGC	GRCh37
NC_000023.9:g.138471495_138471497delinsAGC	NCBI36
NG_007994.1:g.35935_35937delinsAGC , LRG_556:g.35935_35937delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.985_987delinsAGC MANE Select	ENSP00000218099.2:p.Ser329=
ENST00000643157.1:n.1652_1654delinsAGC
ENST00000218099.6:c.985_987delinsAGC	ENSP00000218099.2:p.Ser329=
ENST00000394090.2:c.871_873delinsAGC	ENSP00000377650.2:p.Ser291=
NM_000133.3:c.985_987delinsAGC , LRG_556t1:c.985_987delinsAGC	NP_000124.1:p.Ser329=
NM_001313913.1:c.871_873delinsAGC	NP_001300842.1:p.Ser291=
XM_005262397.3:c.856_858delinsAGC	XP_005262454.1:p.Ser286=
XM_005262397.4:c.856_858delinsAGC	XP_005262454.1:p.Ser286=
NM_000133.4:c.985_987delinsAGC MANE Select	NP_000124.1:p.Ser329=
NM_001313913.2:c.871_873delinsAGC	NP_001300842.1:p.Ser291=