Canonical Allele Identifier: CA2579713827

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560876del , CM000685.2:g.139560876del	GRCh38
NC_000023.10:g.138643035del , CM000685.1:g.138643035del	GRCh37
NC_000023.9:g.138470701del	NCBI36
NG_007994.1:g.35141del , LRG_556:g.35141del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+21del MANE Select	ENSP00000218099.2:n.838+21del
ENST00000643157.1:n.1505+21del
ENST00000218099.6:c.838+21del	ENSP00000218099.2:n.838+21del
ENST00000394090.2:c.724+21del	ENSP00000377650.2:n.724+21del
NM_000133.3:c.838+21del , LRG_556t1:c.838+21del	NP_000124.1:n.838+21del
NM_001313913.1:c.724+21del	NP_001300842.1:n.724+21del
XM_005262397.3:c.709+21del	XP_005262454.1:n.709+21del
XM_005262397.4:c.709+21del	XP_005262454.1:n.709+21del
NM_000133.4:c.838+21del MANE Select	NP_000124.1:n.838+21del
NM_001313913.2:c.724+21del	NP_001300842.1:n.724+21del