Canonical Allele Identifier: CA2694839526

Gene: F9

Linked Data

• gnomAD v4: X-139548241-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548242dup , CM000685.2:g.139548242dup	GRCh38
NC_000023.10:g.138630401dup , CM000685.1:g.138630401dup	GRCh37
NC_000023.9:g.138458067dup	NCBI36
NG_007994.1:g.22507dup , LRG_556:g.22507dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-121dup MANE Select	ENSP00000218099.2:n.392-121dup
ENST00000643157.1:n.1059-121dup
ENST00000218099.6:c.392-121dup	ENSP00000218099.2:n.392-121dup
ENST00000394090.2:c.278-121dup	ENSP00000377650.2:n.278-121dup
ENST00000479617.2:n.345-121dup
NM_000133.3:c.392-121dup , LRG_556t1:c.392-121dup	NP_000124.1:n.392-121dup
NM_001313913.1:c.278-121dup	NP_001300842.1:n.278-121dup
XM_005262397.3:c.392-2820dup	XP_005262454.1:n.392-2820dup
XM_005262397.4:c.392-2820dup	XP_005262454.1:n.392-2820dup
NM_000133.4:c.392-121dup MANE Select	NP_000124.1:n.392-121dup
NM_001313913.2:c.278-121dup	NP_001300842.1:n.278-121dup