Canonical Allele Identifier: CA2695236423

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562044del , CM000685.2:g.139562044del	GRCh38
NC_000023.10:g.138644203del , CM000685.1:g.138644203del	GRCh37
NC_000023.9:g.138471869del	NCBI36
NG_007994.1:g.36309del , LRG_556:g.36309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1359del MANE Select	ENSP00000218099.2:p.Trp453Ter
ENST00000643157.1:n.1723+303del
ENST00000218099.6:c.1359del	ENSP00000218099.2:p.Trp453Ter
ENST00000394090.2:c.1245del	ENSP00000377650.2:p.Trp415Ter
NM_000133.3:c.1359del , LRG_556t1:c.1359del	NP_000124.1:p.Trp453Ter
NM_001313913.1:c.1245del	NP_001300842.1:p.Trp415Ter
XM_005262397.3:c.1230del	XP_005262454.1:p.Trp410Ter
XM_005262397.4:c.1230del	XP_005262454.1:p.Trp410Ter
NM_000133.4:c.1359del MANE Select	NP_000124.1:p.Trp453Ter
NM_001313913.2:c.1245del	NP_001300842.1:p.Trp415Ter