Canonical Allele Identifier: CA3039260806

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561496_139561497insTTC , CM000685.2:g.139561496_139561497insTTC	GRCh38
NC_000023.10:g.138643655_138643656insTTC , CM000685.1:g.138643655_138643656insTTC	GRCh37
NC_000023.9:g.138471321_138471322insTTC	NCBI36
NG_007994.1:g.35761_35762insTTC , LRG_556:g.35761_35762insTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-28_839-27insTTC MANE Select	ENSP00000218099.2:n.839-28_839-27insTTC
ENST00000643157.1:n.1506-28_1506-27insTTC
ENST00000218099.6:c.839-28_839-27insTTC	ENSP00000218099.2:n.839-28_839-27insTTC
ENST00000394090.2:c.725-28_725-27insTTC	ENSP00000377650.2:n.725-28_725-27insTTC
NM_000133.3:c.839-28_839-27insTTC , LRG_556t1:c.839-28_839-27insTTC	NP_000124.1:n.839-28_839-27insTTC
NM_001313913.1:c.725-28_725-27insTTC	NP_001300842.1:n.725-28_725-27insTTC
XM_005262397.3:c.710-28_710-27insTTC	XP_005262454.1:n.710-28_710-27insTTC
XM_005262397.4:c.710-28_710-27insTTC	XP_005262454.1:n.710-28_710-27insTTC
NM_000133.4:c.839-28_839-27insTTC MANE Select	NP_000124.1:n.839-28_839-27insTTC
NM_001313913.2:c.725-28_725-27insTTC	NP_001300842.1:n.725-28_725-27insTTC