Canonical Allele Identifier: CA2695236175

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551088_139551089del , CM000685.2:g.139551088_139551089del	GRCh38
NC_000023.10:g.138633247_138633248del , CM000685.1:g.138633247_138633248del	GRCh37
NC_000023.9:g.138460913_138460914del	NCBI36
NG_007994.1:g.25353_25354del , LRG_556:g.25353_25354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.547_548del MANE Select	ENSP00000218099.2:p.Val183PhefsTer5
ENST00000643157.1:n.1214_1215del
ENST00000218099.6:c.547_548del	ENSP00000218099.2:p.Val183PhefsTer5
ENST00000394090.2:c.433_434del	ENSP00000377650.2:p.Val145PhefsTer5
NM_000133.3:c.547_548del , LRG_556t1:c.547_548del	NP_000124.1:p.Val183PhefsTer5
NM_001313913.1:c.433_434del	NP_001300842.1:p.Val145PhefsTer5
XM_005262397.3:c.418_419del	XP_005262454.1:p.Val140PhefsTer5
XM_005262397.4:c.418_419del	XP_005262454.1:p.Val140PhefsTer5
NM_000133.4:c.547_548del MANE Select	NP_000124.1:p.Val183PhefsTer5
NM_001313913.2:c.433_434del	NP_001300842.1:p.Val145PhefsTer5