Canonical Allele Identifier: CA891862623

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551228_139551230del , CM000685.2:g.139551228_139551230del	GRCh38
NC_000023.10:g.138633387_138633389del , CM000685.1:g.138633387_138633389del	GRCh37
NC_000023.9:g.138461053_138461055del	NCBI36
NG_007994.1:g.25493_25495del , LRG_556:g.25493_25495del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.687_689del MANE Select	ENSP00000218099.2:p.Gly230del
ENST00000643157.1:n.1354_1356del
ENST00000218099.6:c.687_689del	ENSP00000218099.2:p.Gly230del
ENST00000394090.2:c.573_575del	ENSP00000377650.2:p.Gly192del
NM_000133.3:c.687_689del , LRG_556t1:c.687_689del	NP_000124.1:p.Gly230del
NM_001313913.1:c.573_575del	NP_001300842.1:p.Gly192del
XM_005262397.3:c.558_560del	XP_005262454.1:p.Gly187del
XM_005262397.4:c.558_560del	XP_005262454.1:p.Gly187del
NM_000133.4:c.687_689del MANE Select	NP_000124.1:p.Gly230del
NM_001313913.2:c.573_575del	NP_001300842.1:p.Gly192del