Canonical Allele Identifier: CA2579713715

Gene: F9

Linked Data

• gnomAD v4: X-139540980-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139540984del , CM000685.2:g.139540984del	GRCh38
NC_000023.10:g.138623143del , CM000685.1:g.138623143del	GRCh37
NC_000023.9:g.138450809del	NCBI36
NG_007994.1:g.15249del , LRG_556:g.15249del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.278-92del MANE Select	ENSP00000218099.2:n.278-92del
ENST00000218099.6:c.278-92del	ENSP00000218099.2:n.278-92del
ENST00000394090.2:c.277+3598del	ENSP00000377650.2:n.277+3598del
ENST00000479617.2:n.242-103del
NM_000133.3:c.278-92del , LRG_556t1:c.278-92del	NP_000124.1:n.278-92del
NM_001313913.1:c.277+3598del	NP_001300842.1:n.277+3598del
XM_005262397.3:c.278-92del	XP_005262454.1:n.278-92del
XM_005262397.4:c.278-92del	XP_005262454.1:n.278-92del
NM_000133.4:c.278-92del MANE Select	NP_000124.1:n.278-92del
NM_001313913.2:c.277+3598del	NP_001300842.1:n.277+3598del