Canonical Allele Identifier: CA2823819882

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548250del , CM000685.2:g.139548250del	GRCh38
NC_000023.10:g.138630409del , CM000685.1:g.138630409del	GRCh37
NC_000023.9:g.138458075del	NCBI36
NG_007994.1:g.22515del , LRG_556:g.22515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-113del MANE Select	ENSP00000218099.2:n.392-113del
ENST00000643157.1:n.1059-113del
ENST00000218099.6:c.392-113del	ENSP00000218099.2:n.392-113del
ENST00000394090.2:c.278-113del	ENSP00000377650.2:n.278-113del
ENST00000479617.2:n.345-113del
NM_000133.3:c.392-113del , LRG_556t1:c.392-113del	NP_000124.1:n.392-113del
NM_001313913.1:c.278-113del	NP_001300842.1:n.278-113del
XM_005262397.3:c.392-2812del	XP_005262454.1:n.392-2812del
XM_005262397.4:c.392-2812del	XP_005262454.1:n.392-2812del
NM_000133.4:c.392-113del MANE Select	NP_000124.1:n.392-113del
NM_001313913.2:c.278-113del	NP_001300842.1:n.278-113del