Canonical Allele Identifier: CA2695236333

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561753_139561754delinsAA , CM000685.2:g.139561753_139561754delinsAA	GRCh38
NC_000023.10:g.138643912_138643913delinsAA , CM000685.1:g.138643912_138643913delinsAA	GRCh37
NC_000023.9:g.138471578_138471579delinsAA	NCBI36
NG_007994.1:g.36018_36019delinsAA , LRG_556:g.36018_36019delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1068_1069delinsAA MANE Select	ENSP00000218099.2:p.Trp356Ter
ENST00000643157.1:n.1723+12_1723+13delinsAA
ENST00000218099.6:c.1068_1069delinsAA	ENSP00000218099.2:p.Trp356Ter
ENST00000394090.2:c.954_955delinsAA	ENSP00000377650.2:p.Trp318Ter
NM_000133.3:c.1068_1069delinsAA , LRG_556t1:c.1068_1069delinsAA	NP_000124.1:p.Trp356Ter
NM_001313913.1:c.954_955delinsAA	NP_001300842.1:p.Trp318Ter
XM_005262397.3:c.939_940delinsAA	XP_005262454.1:p.Trp313Ter
XM_005262397.4:c.939_940delinsAA	XP_005262454.1:p.Trp313Ter
NM_000133.4:c.1068_1069delinsAA MANE Select	NP_000124.1:p.Trp356Ter
NM_001313913.2:c.954_955delinsAA	NP_001300842.1:p.Trp318Ter