Canonical Allele Identifier: CA2461412188

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561819C= , CM000685.2:g.139561819C=	GRCh38
NC_000023.10:g.138643978C= , CM000685.1:g.138643978C=	GRCh37
NC_000023.9:g.138471644C=	NCBI36
NG_007994.1:g.36084C= , LRG_556:g.36084C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1134C= MANE Select	ENSP00000218099.2:p.Asp378=
ENST00000643157.1:n.1723+78C=
ENST00000218099.6:c.1134C=	ENSP00000218099.2:p.Asp378=
ENST00000394090.2:c.1020C=	ENSP00000377650.2:p.Asp340=
NM_000133.3:c.1134C= , LRG_556t1:c.1134C=	NP_000124.1:p.Asp378=
NM_001313913.1:c.1020C=	NP_001300842.1:p.Asp340=
XM_005262397.3:c.1005C=	XP_005262454.1:p.Asp335=
XM_005262397.4:c.1005C=	XP_005262454.1:p.Asp335=
NM_000133.4:c.1134C= MANE Select	NP_000124.1:p.Asp378=
NM_001313913.2:c.1020C=	NP_001300842.1:p.Asp340=