Canonical Allele Identifier: CA2841394528

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537161_139537165del , CM000685.2:g.139537161_139537165del	GRCh38
NC_000023.10:g.138619320_138619324del , CM000685.1:g.138619320_138619324del	GRCh37
NC_000023.9:g.138446986_138446990del	NCBI36
NG_007994.1:g.11426_11430del , LRG_556:g.11426_11430del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.240_244del MANE Select	ENSP00000218099.2:p.Asn80LysfsTer5
ENST00000218099.6:c.240_244del	ENSP00000218099.2:p.Asn80LysfsTer5
ENST00000394090.2:c.240_244del	ENSP00000377650.2:p.Asn80LysfsTer5
ENST00000479617.2:n.241+6_241+10del
NM_000133.3:c.240_244del , LRG_556t1:c.240_244del	NP_000124.1:p.Asn80LysfsTer5
NM_001313913.1:c.240_244del	NP_001300842.1:p.Asn80LysfsTer5
XM_005262397.3:c.240_244del	XP_005262454.1:p.Asn80LysfsTer5
XM_005262397.4:c.240_244del	XP_005262454.1:p.Asn80LysfsTer5
NM_000133.4:c.240_244del MANE Select	NP_000124.1:p.Asn80LysfsTer5
NM_001313913.2:c.240_244del	NP_001300842.1:p.Asn80LysfsTer5