Canonical Allele Identifier: CA2461412104

Gene: F9

Linked Data

• dbSNP Id: rs1928106601

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561620del , CM000685.2:g.139561620del	GRCh38
NC_000023.10:g.138643779del , CM000685.1:g.138643779del	GRCh37
NC_000023.9:g.138471445del	NCBI36
NG_007994.1:g.35885del , LRG_556:g.35885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.935del MANE Select	ENSP00000218099.2:p.Tyr312SerfsTer14
ENST00000643157.1:n.1602del
ENST00000218099.6:c.935del	ENSP00000218099.2:p.Tyr312SerfsTer14
ENST00000394090.2:c.821del	ENSP00000377650.2:p.Tyr274SerfsTer14
NM_000133.3:c.935del , LRG_556t1:c.935del	NP_000124.1:p.Tyr312SerfsTer14
NM_001313913.1:c.821del	NP_001300842.1:p.Tyr274SerfsTer14
XM_005262397.3:c.806del	XP_005262454.1:p.Tyr269SerfsTer14
XM_005262397.4:c.806del	XP_005262454.1:p.Tyr269SerfsTer14
NM_000133.4:c.935del MANE Select	NP_000124.1:p.Tyr312SerfsTer14
NM_001313913.2:c.821del	NP_001300842.1:p.Tyr274SerfsTer14