Canonical Allele Identifier: CA2695236290

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561617del , CM000685.2:g.139561617del	GRCh38
NC_000023.10:g.138643776del , CM000685.1:g.138643776del	GRCh37
NC_000023.9:g.138471442del	NCBI36
NG_007994.1:g.35882del , LRG_556:g.35882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.932del MANE Select	ENSP00000218099.2:p.Lys311SerfsTer15
ENST00000643157.1:n.1599del
ENST00000218099.6:c.932del	ENSP00000218099.2:p.Lys311SerfsTer15
ENST00000394090.2:c.818del	ENSP00000377650.2:p.Lys273SerfsTer15
NM_000133.3:c.932del , LRG_556t1:c.932del	NP_000124.1:p.Lys311SerfsTer15
NM_001313913.1:c.818del	NP_001300842.1:p.Lys273SerfsTer15
XM_005262397.3:c.803del	XP_005262454.1:p.Lys268SerfsTer15
XM_005262397.4:c.803del	XP_005262454.1:p.Lys268SerfsTer15
NM_000133.4:c.932del MANE Select	NP_000124.1:p.Lys311SerfsTer15
NM_001313913.2:c.818del	NP_001300842.1:p.Lys273SerfsTer15