Canonical Allele Identifier: CA2695236346

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561785del , CM000685.2:g.139561785del	GRCh38
NC_000023.10:g.138643944del , CM000685.1:g.138643944del	GRCh37
NC_000023.9:g.138471610del	NCBI36
NG_007994.1:g.36050del , LRG_556:g.36050del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1100del MANE Select	ENSP00000218099.2:p.Leu367Ter
ENST00000643157.1:n.1723+44del
ENST00000218099.6:c.1100del	ENSP00000218099.2:p.Leu367Ter
ENST00000394090.2:c.986del	ENSP00000377650.2:p.Leu329Ter
NM_000133.3:c.1100del , LRG_556t1:c.1100del	NP_000124.1:p.Leu367Ter
NM_001313913.1:c.986del	NP_001300842.1:p.Leu329Ter
XM_005262397.3:c.971del	XP_005262454.1:p.Leu324Ter
XM_005262397.4:c.971del	XP_005262454.1:p.Leu324Ter
NM_000133.4:c.1100del MANE Select	NP_000124.1:p.Leu367Ter
NM_001313913.2:c.986del	NP_001300842.1:p.Leu329Ter