Canonical Allele Identifier: CA2694839002

Gene: F9

Linked Data

• gnomAD v4: X-139537250-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537254del , CM000685.2:g.139537254del	GRCh38
NC_000023.10:g.138619413del , CM000685.1:g.138619413del	GRCh37
NC_000023.9:g.138447079del	NCBI36
NG_007994.1:g.11519del , LRG_556:g.11519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.252+81del MANE Select	ENSP00000218099.2:n.252+81del
ENST00000218099.6:c.252+81del	ENSP00000218099.2:n.252+81del
ENST00000394090.2:c.252+81del	ENSP00000377650.2:n.252+81del
ENST00000479617.2:n.241+99del
NM_000133.3:c.252+81del , LRG_556t1:c.252+81del	NP_000124.1:n.252+81del
NM_001313913.1:c.252+81del	NP_001300842.1:n.252+81del
XM_005262397.3:c.252+81del	XP_005262454.1:n.252+81del
XM_005262397.4:c.252+81del	XP_005262454.1:n.252+81del
NM_000133.4:c.252+81del MANE Select	NP_000124.1:n.252+81del
NM_001313913.2:c.252+81del	NP_001300842.1:n.252+81del