Canonical Allele Identifier: CA2695236385

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561898_139561899del , CM000685.2:g.139561898_139561899del	GRCh38
NC_000023.10:g.138644057_138644058del , CM000685.1:g.138644057_138644058del	GRCh37
NC_000023.9:g.138471723_138471724del	NCBI36
NG_007994.1:g.36163_36164del , LRG_556:g.36163_36164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1213_1214del MANE Select	ENSP00000218099.2:p.Asp405PhefsTer6
ENST00000643157.1:n.1723+157_1723+158del
ENST00000218099.6:c.1213_1214del	ENSP00000218099.2:p.Asp405PhefsTer6
ENST00000394090.2:c.1099_1100del	ENSP00000377650.2:p.Asp367PhefsTer6
NM_000133.3:c.1213_1214del , LRG_556t1:c.1213_1214del	NP_000124.1:p.Asp405PhefsTer6
NM_001313913.1:c.1099_1100del	NP_001300842.1:p.Asp367PhefsTer6
XM_005262397.3:c.1084_1085del	XP_005262454.1:p.Asp362PhefsTer6
XM_005262397.4:c.1084_1085del	XP_005262454.1:p.Asp362PhefsTer6
NM_000133.4:c.1213_1214del MANE Select	NP_000124.1:p.Asp405PhefsTer6
NM_001313913.2:c.1099_1100del	NP_001300842.1:p.Asp367PhefsTer6