Canonical Allele Identifier: CA2695236229

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560760_139560762del , CM000685.2:g.139560760_139560762del	GRCh38
NC_000023.10:g.138642919_138642921del , CM000685.1:g.138642919_138642921del	GRCh37
NC_000023.9:g.138470585_138470587del	NCBI36
NG_007994.1:g.35025_35027del , LRG_556:g.35025_35027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.743_745del MANE Select	ENSP00000218099.2:p.Val248del
ENST00000643157.1:n.1410_1412del
ENST00000218099.6:c.743_745del	ENSP00000218099.2:p.Val248del
ENST00000394090.2:c.629_631del	ENSP00000377650.2:p.Val210del
NM_000133.3:c.743_745del , LRG_556t1:c.743_745del	NP_000124.1:p.Val248del
NM_001313913.1:c.629_631del	NP_001300842.1:p.Val210del
XM_005262397.3:c.614_616del	XP_005262454.1:p.Val205del
XM_005262397.4:c.614_616del	XP_005262454.1:p.Val205del
NM_000133.4:c.743_745del MANE Select	NP_000124.1:p.Val248del
NM_001313913.2:c.629_631del	NP_001300842.1:p.Val210del