Canonical Allele Identifier: CA2695236371

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561861_139561865del , CM000685.2:g.139561861_139561865del	GRCh38
NC_000023.10:g.138644020_138644024del , CM000685.1:g.138644020_138644024del	GRCh37
NC_000023.9:g.138471686_138471690del	NCBI36
NG_007994.1:g.36126_36130del , LRG_556:g.36126_36130del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1176_1180del MANE Select	ENSP00000218099.2:p.Asn393ValfsTer7
ENST00000643157.1:n.1723+120_1723+124del
ENST00000218099.6:c.1176_1180del	ENSP00000218099.2:p.Asn393ValfsTer7
ENST00000394090.2:c.1062_1066del	ENSP00000377650.2:p.Asn355ValfsTer7
NM_000133.3:c.1176_1180del , LRG_556t1:c.1176_1180del	NP_000124.1:p.Asn393ValfsTer7
NM_001313913.1:c.1062_1066del	NP_001300842.1:p.Asn355ValfsTer7
XM_005262397.3:c.1047_1051del	XP_005262454.1:p.Asn350ValfsTer7
XM_005262397.4:c.1047_1051del	XP_005262454.1:p.Asn350ValfsTer7
NM_000133.4:c.1176_1180del MANE Select	NP_000124.1:p.Asn393ValfsTer7
NM_001313913.2:c.1062_1066del	NP_001300842.1:p.Asn355ValfsTer7