Canonical Allele Identifier: CA2695236193

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551168del , CM000685.2:g.139551168del	GRCh38
NC_000023.10:g.138633327del , CM000685.1:g.138633327del	GRCh37
NC_000023.9:g.138460993del	NCBI36
NG_007994.1:g.25433del , LRG_556:g.25433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.627del MANE Select	ENSP00000218099.2:p.Ile210PhefsTer?
ENST00000643157.1:n.1294del
ENST00000218099.6:c.627del	ENSP00000218099.2:p.Ile210PhefsTer?
ENST00000394090.2:c.513del	ENSP00000377650.2:p.Ile172PhefsTer?
NM_000133.3:c.627del , LRG_556t1:c.627del	NP_000124.1:p.Ile210PhefsTer?
NM_001313913.1:c.513del	NP_001300842.1:p.Ile172PhefsTer?
XM_005262397.3:c.498del	XP_005262454.1:p.Ile167PhefsTer?
XM_005262397.4:c.498del	XP_005262454.1:p.Ile167PhefsTer?
NM_000133.4:c.627del MANE Select	NP_000124.1:p.Ile210PhefsTer?
NM_001313913.2:c.513del	NP_001300842.1:p.Ile172PhefsTer?