Canonical Allele Identifier: CA2695236345

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561785_139561792del , CM000685.2:g.139561785_139561792del	GRCh38
NC_000023.10:g.138643944_138643951del , CM000685.1:g.138643944_138643951del	GRCh37
NC_000023.9:g.138471610_138471617del	NCBI36
NG_007994.1:g.36050_36057del , LRG_556:g.36050_36057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1100_1107del MANE Select	ENSP00000218099.2:p.Leu367SerfsTer4
ENST00000643157.1:n.1723+44_1723+51del
ENST00000218099.6:c.1100_1107del	ENSP00000218099.2:p.Leu367SerfsTer4
ENST00000394090.2:c.986_993del	ENSP00000377650.2:p.Leu329SerfsTer4
NM_000133.3:c.1100_1107del , LRG_556t1:c.1100_1107del	NP_000124.1:p.Leu367SerfsTer4
NM_001313913.1:c.986_993del	NP_001300842.1:p.Leu329SerfsTer4
XM_005262397.3:c.971_978del	XP_005262454.1:p.Leu324SerfsTer4
XM_005262397.4:c.971_978del	XP_005262454.1:p.Leu324SerfsTer4
NM_000133.4:c.1100_1107del MANE Select	NP_000124.1:p.Leu367SerfsTer4
NM_001313913.2:c.986_993del	NP_001300842.1:p.Leu329SerfsTer4