Canonical Allele Identifier: CA2695236353
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561819_139561820delinsAACTCTAA , CM000685.2:g.139561819_139561820delinsAACTCTAA GRCh38
NC_000023.10:g.138643978_138643979delinsAACTCTAA , CM000685.1:g.138643978_138643979delinsAACTCTAA GRCh37
NC_000023.9:g.138471644_138471645delinsAACTCTAA NCBI36
NG_007994.1:g.36084_36085delinsAACTCTAA , LRG_556:g.36084_36085delinsAACTCTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1134_1135delinsAACTCTAA MANE Select ENSP00000218099.2:p.Asp378delinsGluThrLeu...
ENST00000643157.1:n.1723+78_1723+79delinsAACTCTAA
ENST00000218099.6:c.1134_1135delinsAACTCTAA ENSP00000218099.2:p.Asp378delinsGluThrLeu...
ENST00000394090.2:c.1020_1021delinsAACTCTAA ENSP00000377650.2:p.Asp340delinsGluThrLeu...
NM_000133.3:c.1134_1135delinsAACTCTAA , LRG_556t1:c.1134_1135delinsAACTCTAA NP_000124.1:p.Asp378delinsGluThrLeu
NM_001313913.1:c.1020_1021delinsAACTCTAA NP_001300842.1:p.Asp340delinsGluThrLeu
XM_005262397.3:c.1005_1006delinsAACTCTAA XP_005262454.1:p.Asp335delinsGluThrLeu
XM_005262397.4:c.1005_1006delinsAACTCTAA XP_005262454.1:p.Asp335delinsGluThrLeu
NM_000133.4:c.1134_1135delinsAACTCTAA MANE Select NP_000124.1:p.Asp378delinsGluThrLeu
NM_001313913.2:c.1020_1021delinsAACTCTAA NP_001300842.1:p.Asp340delinsGluThrLeu