Canonical Allele Identifier: CA2695236255

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560830_139560831del , CM000685.2:g.139560830_139560831del	GRCh38
NC_000023.10:g.138642989_138642990del , CM000685.1:g.138642989_138642990del	GRCh37
NC_000023.9:g.138470655_138470656del	NCBI36
NG_007994.1:g.35095_35096del , LRG_556:g.35095_35096del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.813_814del MANE Select	ENSP00000218099.2:p.Gly272CysfsTer2
ENST00000643157.1:n.1480_1481del
ENST00000218099.6:c.813_814del	ENSP00000218099.2:p.Gly272CysfsTer2
ENST00000394090.2:c.699_700del	ENSP00000377650.2:p.Gly234CysfsTer2
NM_000133.3:c.813_814del , LRG_556t1:c.813_814del	NP_000124.1:p.Gly272CysfsTer2
NM_001313913.1:c.699_700del	NP_001300842.1:p.Gly234CysfsTer2
XM_005262397.3:c.684_685del	XP_005262454.1:p.Gly229CysfsTer2
XM_005262397.4:c.684_685del	XP_005262454.1:p.Gly229CysfsTer2
NM_000133.4:c.813_814del MANE Select	NP_000124.1:p.Gly272CysfsTer2
NM_001313913.2:c.699_700del	NP_001300842.1:p.Gly234CysfsTer2