Canonical Allele Identifier: CA2841394530

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537169_139537170insTA , CM000685.2:g.139537169_139537170insTA	GRCh38
NC_000023.10:g.138619328_138619329insTA , CM000685.1:g.138619328_138619329insTA	GRCh37
NC_000023.9:g.138446994_138446995insTA	NCBI36
NG_007994.1:g.11434_11435insTA , LRG_556:g.11434_11435insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.248_249insTA MANE Select	ENSP00000218099.2:p.Arg83SerfsTer22
ENST00000218099.6:c.248_249insTA	ENSP00000218099.2:p.Arg83SerfsTer22
ENST00000394090.2:c.248_249insTA	ENSP00000377650.2:p.Arg83SerfsTer13
ENST00000479617.2:n.241+14_241+15insTA
NM_000133.3:c.248_249insTA , LRG_556t1:c.248_249insTA	NP_000124.1:p.Arg83SerfsTer22
NM_001313913.1:c.248_249insTA	NP_001300842.1:p.Arg83SerfsTer13
XM_005262397.3:c.248_249insTA	XP_005262454.1:p.Arg83SerfsTer22
XM_005262397.4:c.248_249insTA	XP_005262454.1:p.Arg83SerfsTer22
NM_000133.4:c.248_249insTA MANE Select	NP_000124.1:p.Arg83SerfsTer22
NM_001313913.2:c.248_249insTA	NP_001300842.1:p.Arg83SerfsTer13