Canonical Allele Identifier: CA2579713729

Gene: F9

Linked Data

• gnomAD v4: X-139541032-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541034del , CM000685.2:g.139541034del	GRCh38
NC_000023.10:g.138623193del , CM000685.1:g.138623193del	GRCh37
NC_000023.9:g.138450859del	NCBI36
NG_007994.1:g.15299del , LRG_556:g.15299del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.278-42del MANE Select	ENSP00000218099.2:n.278-42del
ENST00000218099.6:c.278-42del	ENSP00000218099.2:n.278-42del
ENST00000394090.2:c.277+3648del	ENSP00000377650.2:n.277+3648del
ENST00000479617.2:n.242-53del
NM_000133.3:c.278-42del , LRG_556t1:c.278-42del	NP_000124.1:n.278-42del
NM_001313913.1:c.277+3648del	NP_001300842.1:n.277+3648del
XM_005262397.3:c.278-42del	XP_005262454.1:n.278-42del
XM_005262397.4:c.278-42del	XP_005262454.1:n.278-42del
NM_000133.4:c.278-42del MANE Select	NP_000124.1:n.278-42del
NM_001313913.2:c.277+3648del	NP_001300842.1:n.277+3648del