Canonical Allele Identifier: CA2695236173

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551081del , CM000685.2:g.139551081del	GRCh38
NC_000023.10:g.138633240del , CM000685.1:g.138633240del	GRCh37
NC_000023.9:g.138460906del	NCBI36
NG_007994.1:g.25346del , LRG_556:g.25346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.540del MANE Select	ENSP00000218099.2:p.Val181PhefsTer22
ENST00000643157.1:n.1207del
ENST00000218099.6:c.540del	ENSP00000218099.2:p.Val181PhefsTer22
ENST00000394090.2:c.426del	ENSP00000377650.2:p.Val143PhefsTer22
NM_000133.3:c.540del , LRG_556t1:c.540del	NP_000124.1:p.Val181PhefsTer22
NM_001313913.1:c.426del	NP_001300842.1:p.Val143PhefsTer22
XM_005262397.3:c.411del	XP_005262454.1:p.Val138PhefsTer22
XM_005262397.4:c.411del	XP_005262454.1:p.Val138PhefsTer22
NM_000133.4:c.540del MANE Select	NP_000124.1:p.Val181PhefsTer22
NM_001313913.2:c.426del	NP_001300842.1:p.Val143PhefsTer22