Canonical Allele Identifier: CA872122272

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551086_139551087del , CM000685.2:g.139551086_139551087del	GRCh38
NC_000023.10:g.138633245_138633246del , CM000685.1:g.138633245_138633246del	GRCh37
NC_000023.9:g.138460911_138460912del	NCBI36
NG_007994.1:g.25351_25352del , LRG_556:g.25351_25352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.545_546del MANE Select	ENSP00000218099.2:p.Ser182CysfsTer6
ENST00000643157.1:n.1212_1213del
ENST00000218099.6:c.545_546del	ENSP00000218099.2:p.Ser182CysfsTer6
ENST00000394090.2:c.431_432del	ENSP00000377650.2:p.Ser144CysfsTer6
NM_000133.3:c.545_546del , LRG_556t1:c.545_546del	NP_000124.1:p.Ser182CysfsTer6
NM_001313913.1:c.431_432del	NP_001300842.1:p.Ser144CysfsTer6
XM_005262397.3:c.416_417del	XP_005262454.1:p.Ser139CysfsTer6
XM_005262397.4:c.416_417del	XP_005262454.1:p.Ser139CysfsTer6
NM_000133.4:c.545_546del MANE Select	NP_000124.1:p.Ser182CysfsTer6
NM_001313913.2:c.431_432del	NP_001300842.1:p.Ser144CysfsTer6