Canonical Allele Identifier: CA3039260801

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561487del , CM000685.2:g.139561487del	GRCh38
NC_000023.10:g.138643646del , CM000685.1:g.138643646del	GRCh37
NC_000023.9:g.138471312del	NCBI36
NG_007994.1:g.35752del , LRG_556:g.35752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-37del MANE Select	ENSP00000218099.2:n.839-37del
ENST00000643157.1:n.1506-37del
ENST00000218099.6:c.839-37del	ENSP00000218099.2:n.839-37del
ENST00000394090.2:c.725-37del	ENSP00000377650.2:n.725-37del
NM_000133.3:c.839-37del , LRG_556t1:c.839-37del	NP_000124.1:n.839-37del
NM_001313913.1:c.725-37del	NP_001300842.1:n.725-37del
XM_005262397.3:c.710-37del	XP_005262454.1:n.710-37del
XM_005262397.4:c.710-37del	XP_005262454.1:n.710-37del
NM_000133.4:c.839-37del MANE Select	NP_000124.1:n.839-37del
NM_001313913.2:c.725-37del	NP_001300842.1:n.725-37del