Canonical Allele Identifier: CA2695236196

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551187_139551188del , CM000685.2:g.139551187_139551188del	GRCh38
NC_000023.10:g.138633346_138633347del , CM000685.1:g.138633346_138633347del	GRCh37
NC_000023.9:g.138461012_138461013del	NCBI36
NG_007994.1:g.25452_25453del , LRG_556:g.25452_25453del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.646_647del MANE Select	ENSP00000218099.2:p.Gln216LysfsTer6
ENST00000643157.1:n.1313_1314del
ENST00000218099.6:c.646_647del	ENSP00000218099.2:p.Gln216LysfsTer6
ENST00000394090.2:c.532_533del	ENSP00000377650.2:p.Gln178LysfsTer6
NM_000133.3:c.646_647del , LRG_556t1:c.646_647del	NP_000124.1:p.Gln216LysfsTer6
NM_001313913.1:c.532_533del	NP_001300842.1:p.Gln178LysfsTer6
XM_005262397.3:c.517_518del	XP_005262454.1:p.Gln173LysfsTer6
XM_005262397.4:c.517_518del	XP_005262454.1:p.Gln173LysfsTer6
NM_000133.4:c.646_647del MANE Select	NP_000124.1:p.Gln216LysfsTer6
NM_001313913.2:c.532_533del	NP_001300842.1:p.Gln178LysfsTer6