Canonical Allele Identifier: CA2695236294

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561625del , CM000685.2:g.139561625del	GRCh38
NC_000023.10:g.138643784del , CM000685.1:g.138643784del	GRCh37
NC_000023.9:g.138471450del	NCBI36
NG_007994.1:g.35890del , LRG_556:g.35890del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.940del MANE Select	ENSP00000218099.2:p.His314MetfsTer12
ENST00000643157.1:n.1607del
ENST00000218099.6:c.940del	ENSP00000218099.2:p.His314MetfsTer12
ENST00000394090.2:c.826del	ENSP00000377650.2:p.His276MetfsTer12
NM_000133.3:c.940del , LRG_556t1:c.940del	NP_000124.1:p.His314MetfsTer12
NM_001313913.1:c.826del	NP_001300842.1:p.His276MetfsTer12
XM_005262397.3:c.811del	XP_005262454.1:p.His271MetfsTer12
XM_005262397.4:c.811del	XP_005262454.1:p.His271MetfsTer12
NM_000133.4:c.940del MANE Select	NP_000124.1:p.His314MetfsTer12
NM_001313913.2:c.826del	NP_001300842.1:p.His276MetfsTer12