Canonical Allele Identifier: CA2695236375

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561865del , CM000685.2:g.139561865del	GRCh38
NC_000023.10:g.138644024del , CM000685.1:g.138644024del	GRCh37
NC_000023.9:g.138471690del	NCBI36
NG_007994.1:g.36130del , LRG_556:g.36130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1180del MANE Select	ENSP00000218099.2:p.Met394CysfsTer?
ENST00000643157.1:n.1723+124del
ENST00000218099.6:c.1180del	ENSP00000218099.2:p.Met394CysfsTer?
ENST00000394090.2:c.1066del	ENSP00000377650.2:p.Met356CysfsTer?
NM_000133.3:c.1180del , LRG_556t1:c.1180del	NP_000124.1:p.Met394CysfsTer?
NM_001313913.1:c.1066del	NP_001300842.1:p.Met356CysfsTer?
XM_005262397.3:c.1051del	XP_005262454.1:p.Met351CysfsTer?
XM_005262397.4:c.1051del	XP_005262454.1:p.Met351CysfsTer?
NM_000133.4:c.1180del MANE Select	NP_000124.1:p.Met394CysfsTer?
NM_001313913.2:c.1066del	NP_001300842.1:p.Met356CysfsTer?