Canonical Allele Identifier: CA2695236403

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548478_139548480delinsTTT , CM000685.2:g.139548478_139548480delinsTTT	GRCh38
NC_000023.10:g.138630637_138630639delinsTTT , CM000685.1:g.138630637_138630639delinsTTT	GRCh37
NC_000023.9:g.138458303_138458305delinsTTT	NCBI36
NG_007994.1:g.22743_22745delinsTTT , LRG_556:g.22743_22745delinsTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.507_509delinsTTT MANE Select	ENSP00000218099.2:p.Cys170Phe
ENST00000643157.1:n.1174_1176delinsTTT
ENST00000218099.6:c.507_509delinsTTT	ENSP00000218099.2:p.Cys170Phe
ENST00000394090.2:c.393_395delinsTTT	ENSP00000377650.2:p.Cys132Phe
NM_000133.3:c.507_509delinsTTT , LRG_556t1:c.507_509delinsTTT	NP_000124.1:p.Cys170Phe
NM_001313913.1:c.393_395delinsTTT	NP_001300842.1:p.Cys132Phe
XM_005262397.3:c.392-2584_392-2582delinsTTT	XP_005262454.1:n.392-2584_392-2582delinsT...
XM_005262397.4:c.392-2584_392-2582delinsTTT	XP_005262454.1:n.392-2584_392-2582delinsT...
NM_000133.4:c.507_509delinsTTT MANE Select	NP_000124.1:p.Cys170Phe
NM_001313913.2:c.393_395delinsTTT	NP_001300842.1:p.Cys132Phe