Canonical Allele Identifier: CA2695236328

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561744_139561753del , CM000685.2:g.139561744_139561753del	GRCh38
NC_000023.10:g.138643903_138643912del , CM000685.1:g.138643903_138643912del	GRCh37
NC_000023.9:g.138471569_138471578del	NCBI36
NG_007994.1:g.36009_36018del , LRG_556:g.36009_36018del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1059_1068del MANE Select	ENSP00000218099.2:p.Ser354GlufsTer11
ENST00000643157.1:n.1723+3_1723+12del
ENST00000218099.6:c.1059_1068del	ENSP00000218099.2:p.Ser354GlufsTer11
ENST00000394090.2:c.945_954del	ENSP00000377650.2:p.Ser316GlufsTer11
NM_000133.3:c.1059_1068del , LRG_556t1:c.1059_1068del	NP_000124.1:p.Ser354GlufsTer11
NM_001313913.1:c.945_954del	NP_001300842.1:p.Ser316GlufsTer11
XM_005262397.3:c.930_939del	XP_005262454.1:p.Ser311GlufsTer11
XM_005262397.4:c.930_939del	XP_005262454.1:p.Ser311GlufsTer11
NM_000133.4:c.1059_1068del MANE Select	NP_000124.1:p.Ser354GlufsTer11
NM_001313913.2:c.945_954del	NP_001300842.1:p.Ser316GlufsTer11