Canonical Allele Identifier: CA255422

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562042T>C , CM000685.2:g.139562042T>C	GRCh38
NC_000023.10:g.138644201T>C , CM000685.1:g.138644201T>C	GRCh37
NC_000023.9:g.138471867T>C	NCBI36
NG_007994.1:g.36307T>C , LRG_556:g.36307T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.1357T>C MANE Select	NP_000124.1:p.Trp453Arg
ENST00000218099.7:c.1357T>C MANE Select	ENSP00000218099.2:p.Trp453Arg
NM_000133.3:c.1357T>C , LRG_556t1:c.1357T>C	NP_000124.1:p.Trp453Arg
NM_001313913.1:c.1243T>C	NP_001300842.1:p.Trp415Arg
NM_001313913.2:c.1243T>C	NP_001300842.1:p.Trp415Arg
ENST00000218099.6:c.1357T>C	ENSP00000218099.2:p.Trp453Arg
ENST00000394090.2:c.1243T>C	ENSP00000377650.2:p.Trp415Arg
ENST00000643157.1:n.1723+301T>C
XM_005262397.3:c.1228T>C	XP_005262454.1:p.Trp410Arg
XM_005262397.4:c.1228T>C	XP_005262454.1:p.Trp410Arg