Canonical Allele Identifier: CA2695236318

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561709_139561710dup , CM000685.2:g.139561709_139561710dup	GRCh38
NC_000023.10:g.138643868_138643869dup , CM000685.1:g.138643868_138643869dup	GRCh37
NC_000023.9:g.138471534_138471535dup	NCBI36
NG_007994.1:g.35974_35975dup , LRG_556:g.35974_35975dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1024_1025dup MANE Select	ENSP00000218099.2:p.Asn343ArgfsTer12
ENST00000643157.1:n.1691_1692dup
ENST00000218099.6:c.1024_1025dup	ENSP00000218099.2:p.Asn343ArgfsTer12
ENST00000394090.2:c.910_911dup	ENSP00000377650.2:p.Asn305ArgfsTer12
NM_000133.3:c.1024_1025dup , LRG_556t1:c.1024_1025dup	NP_000124.1:p.Asn343ArgfsTer12
NM_001313913.1:c.910_911dup	NP_001300842.1:p.Asn305ArgfsTer12
XM_005262397.3:c.895_896dup	XP_005262454.1:p.Asn300ArgfsTer12
XM_005262397.4:c.895_896dup	XP_005262454.1:p.Asn300ArgfsTer12
NM_000133.4:c.1024_1025dup MANE Select	NP_000124.1:p.Asn343ArgfsTer12
NM_001313913.2:c.910_911dup	NP_001300842.1:p.Asn305ArgfsTer12