Canonical Allele Identifier: CA2695236279

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561559del , CM000685.2:g.139561559del	GRCh38
NC_000023.10:g.138643718del , CM000685.1:g.138643718del	GRCh37
NC_000023.9:g.138471384del	NCBI36
NG_007994.1:g.35824del , LRG_556:g.35824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.874del MANE Select	ENSP00000218099.2:p.Gln292LysfsTer5
ENST00000643157.1:n.1541del
ENST00000218099.6:c.874del	ENSP00000218099.2:p.Gln292LysfsTer5
ENST00000394090.2:c.760del	ENSP00000377650.2:p.Gln254LysfsTer5
NM_000133.3:c.874del , LRG_556t1:c.874del	NP_000124.1:p.Gln292LysfsTer5
NM_001313913.1:c.760del	NP_001300842.1:p.Gln254LysfsTer5
XM_005262397.3:c.745del	XP_005262454.1:p.Gln249LysfsTer5
XM_005262397.4:c.745del	XP_005262454.1:p.Gln249LysfsTer5
NM_000133.4:c.874del MANE Select	NP_000124.1:p.Gln292LysfsTer5
NM_001313913.2:c.760del	NP_001300842.1:p.Gln254LysfsTer5