Canonical Allele Identifier: CA2695236343

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561780del , CM000685.2:g.139561780del	GRCh38
NC_000023.10:g.138643939del , CM000685.1:g.138643939del	GRCh37
NC_000023.9:g.138471605del	NCBI36
NG_007994.1:g.36045del , LRG_556:g.36045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1095del MANE Select	ENSP00000218099.2:p.Ala366LeufsTer2
ENST00000643157.1:n.1723+39del
ENST00000218099.6:c.1095del	ENSP00000218099.2:p.Ala366LeufsTer2
ENST00000394090.2:c.981del	ENSP00000377650.2:p.Ala328LeufsTer2
NM_000133.3:c.1095del , LRG_556t1:c.1095del	NP_000124.1:p.Ala366LeufsTer2
NM_001313913.1:c.981del	NP_001300842.1:p.Ala328LeufsTer2
XM_005262397.3:c.966del	XP_005262454.1:p.Ala323LeufsTer2
XM_005262397.4:c.966del	XP_005262454.1:p.Ala323LeufsTer2
NM_000133.4:c.1095del MANE Select	NP_000124.1:p.Ala366LeufsTer2
NM_001313913.2:c.981del	NP_001300842.1:p.Ala328LeufsTer2