Canonical Allele Identifier: CA2695236359

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561834dup , CM000685.2:g.139561834dup	GRCh38
NC_000023.10:g.138643993dup , CM000685.1:g.138643993dup	GRCh37
NC_000023.9:g.138471659dup	NCBI36
NG_007994.1:g.36099dup , LRG_556:g.36099dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1149dup MANE Select	ENSP00000218099.2:p.Arg384SerfsTer9
ENST00000643157.1:n.1723+93dup
ENST00000218099.6:c.1149dup	ENSP00000218099.2:p.Arg384SerfsTer9
ENST00000394090.2:c.1035dup	ENSP00000377650.2:p.Arg346SerfsTer9
NM_000133.3:c.1149dup , LRG_556t1:c.1149dup	NP_000124.1:p.Arg384SerfsTer9
NM_001313913.1:c.1035dup	NP_001300842.1:p.Arg346SerfsTer9
XM_005262397.3:c.1020dup	XP_005262454.1:p.Arg341SerfsTer9
XM_005262397.4:c.1020dup	XP_005262454.1:p.Arg341SerfsTer9
NM_000133.4:c.1149dup MANE Select	NP_000124.1:p.Arg384SerfsTer9
NM_001313913.2:c.1035dup	NP_001300842.1:p.Arg346SerfsTer9