Canonical Allele Identifier: CA2695236413

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561989_139561990insAG , CM000685.2:g.139561989_139561990insAG	GRCh38
NC_000023.10:g.138644148_138644149insAG , CM000685.1:g.138644148_138644149insAG	GRCh37
NC_000023.9:g.138471814_138471815insAG	NCBI36
NG_007994.1:g.36254_36255insAG , LRG_556:g.36254_36255insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1304_1305insAG MANE Select	ENSP00000218099.2:p.Cys435Ter
ENST00000643157.1:n.1723+248_1723+249insAG
ENST00000218099.6:c.1304_1305insAG	ENSP00000218099.2:p.Cys435Ter
ENST00000394090.2:c.1190_1191insAG	ENSP00000377650.2:p.Cys397Ter
NM_000133.3:c.1304_1305insAG , LRG_556t1:c.1304_1305insAG	NP_000124.1:p.Cys435Ter
NM_001313913.1:c.1190_1191insAG	NP_001300842.1:p.Cys397Ter
XM_005262397.3:c.1175_1176insAG	XP_005262454.1:p.Cys392Ter
XM_005262397.4:c.1175_1176insAG	XP_005262454.1:p.Cys392Ter
NM_000133.4:c.1304_1305insAG MANE Select	NP_000124.1:p.Cys435Ter
NM_001313913.2:c.1190_1191insAG	NP_001300842.1:p.Cys397Ter