Canonical Allele Identifier: CA2461408588

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551064C= , CM000685.2:g.139551064C=	GRCh38
NC_000023.10:g.138633223C= , CM000685.1:g.138633223C=	GRCh37
NC_000023.9:g.138460889C=	NCBI36
NG_007994.1:g.25329C= , LRG_556:g.25329C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.523C= MANE Select	ENSP00000218099.2:p.Pro175=
ENST00000643157.1:n.1190C=
ENST00000218099.6:c.523C=	ENSP00000218099.2:p.Pro175=
ENST00000394090.2:c.409C=	ENSP00000377650.2:p.Pro137=
NM_000133.3:c.523C= , LRG_556t1:c.523C=	NP_000124.1:p.Pro175=
NM_001313913.1:c.409C=	NP_001300842.1:p.Pro137=
XM_005262397.3:c.394C=	XP_005262454.1:p.Pro132=
XM_005262397.4:c.394C=	XP_005262454.1:p.Pro132=
NM_000133.4:c.523C= MANE Select	NP_000124.1:p.Pro175=
NM_001313913.2:c.409C=	NP_001300842.1:p.Pro137=