Canonical Allele Identifier: CA2695236390
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561917_139561919delinsTT , CM000685.2:g.139561917_139561919delinsTT GRCh38
NC_000023.10:g.138644076_138644078delinsTT , CM000685.1:g.138644076_138644078delinsTT GRCh37
NC_000023.9:g.138471742_138471744delinsTT NCBI36
NG_007994.1:g.36182_36184delinsTT , LRG_556:g.36182_36184delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1232_1234delinsTT MANE Select ENSP00000218099.2:p.Ser411IlefsTer15
ENST00000643157.1:n.1723+176_1723+178delinsTT
ENST00000218099.6:c.1232_1234delinsTT ENSP00000218099.2:p.Ser411IlefsTer15
ENST00000394090.2:c.1118_1120delinsTT ENSP00000377650.2:p.Ser373IlefsTer15
NM_000133.3:c.1232_1234delinsTT , LRG_556t1:c.1232_1234delinsTT NP_000124.1:p.Ser411IlefsTer15
NM_001313913.1:c.1118_1120delinsTT NP_001300842.1:p.Ser373IlefsTer15
XM_005262397.3:c.1103_1105delinsTT XP_005262454.1:p.Ser368IlefsTer15
XM_005262397.4:c.1103_1105delinsTT XP_005262454.1:p.Ser368IlefsTer15
NM_000133.4:c.1232_1234delinsTT MANE Select NP_000124.1:p.Ser411IlefsTer15
NM_001313913.2:c.1118_1120delinsTT NP_001300842.1:p.Ser373IlefsTer15