Canonical Allele Identifier: CA2461412276

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561977G= , CM000685.2:g.139561977G=	GRCh38
NC_000023.10:g.138644136G= , CM000685.1:g.138644136G=	GRCh37
NC_000023.9:g.138471802G=	NCBI36
NG_007994.1:g.36242G= , LRG_556:g.36242G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1292G= MANE Select	ENSP00000218099.2:p.Trp431=
ENST00000643157.1:n.1723+236G=
ENST00000218099.6:c.1292G=	ENSP00000218099.2:p.Trp431=
ENST00000394090.2:c.1178G=	ENSP00000377650.2:p.Trp393=
NM_000133.3:c.1292G= , LRG_556t1:c.1292G=	NP_000124.1:p.Trp431=
NM_001313913.1:c.1178G=	NP_001300842.1:p.Trp393=
XM_005262397.3:c.1163G=	XP_005262454.1:p.Trp388=
XM_005262397.4:c.1163G=	XP_005262454.1:p.Trp388=
NM_000133.4:c.1292G= MANE Select	NP_000124.1:p.Trp431=
NM_001313913.2:c.1178G=	NP_001300842.1:p.Trp393=