Canonical Allele Identifier: CA2695236200

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551208_139551212del , CM000685.2:g.139551208_139551212del	GRCh38
NC_000023.10:g.138633367_138633371del , CM000685.1:g.138633367_138633371del	GRCh37
NC_000023.9:g.138461033_138461037del	NCBI36
NG_007994.1:g.25473_25477del , LRG_556:g.25473_25477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.667_671del MANE Select	ENSP00000218099.2:p.Asp223HisfsTer23
ENST00000643157.1:n.1334_1338del
ENST00000218099.6:c.667_671del	ENSP00000218099.2:p.Asp223HisfsTer23
ENST00000394090.2:c.553_557del	ENSP00000377650.2:p.Asp185HisfsTer23
NM_000133.3:c.667_671del , LRG_556t1:c.667_671del	NP_000124.1:p.Asp223HisfsTer23
NM_001313913.1:c.553_557del	NP_001300842.1:p.Asp185HisfsTer23
XM_005262397.3:c.538_542del	XP_005262454.1:p.Asp180HisfsTer23
XM_005262397.4:c.538_542del	XP_005262454.1:p.Asp180HisfsTer23
NM_000133.4:c.667_671del MANE Select	NP_000124.1:p.Asp223HisfsTer23
NM_001313913.2:c.553_557del	NP_001300842.1:p.Asp185HisfsTer23