Canonical Allele Identifier: CA2694839518

Gene: F9

Linked Data

• gnomAD v4: X-139548231-TCCCCAACGTATATTGGGGGCAACATGAATGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548238_139548268del , CM000685.2:g.139548238_139548268del	GRCh38
NC_000023.10:g.138630397_138630427del , CM000685.1:g.138630397_138630427del	GRCh37
NC_000023.9:g.138458063_138458093del	NCBI36
NG_007994.1:g.22503_22533del , LRG_556:g.22503_22533del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-125_392-95del MANE Select	ENSP00000218099.2:n.392-125_392-95del
ENST00000643157.1:n.1059-125_1059-95del
ENST00000218099.6:c.392-125_392-95del	ENSP00000218099.2:n.392-125_392-95del
ENST00000394090.2:c.278-125_278-95del	ENSP00000377650.2:n.278-125_278-95del
ENST00000479617.2:n.345-125_345-95del
NM_000133.3:c.392-125_392-95del , LRG_556t1:c.392-125_392-95del	NP_000124.1:n.392-125_392-95del
NM_001313913.1:c.278-125_278-95del	NP_001300842.1:n.278-125_278-95del
XM_005262397.3:c.392-2824_392-2794del	XP_005262454.1:n.392-2824_392-2794del
XM_005262397.4:c.392-2824_392-2794del	XP_005262454.1:n.392-2824_392-2794del
NM_000133.4:c.392-125_392-95del MANE Select	NP_000124.1:n.392-125_392-95del
NM_001313913.2:c.278-125_278-95del	NP_001300842.1:n.278-125_278-95del