Canonical Allele Identifier: CA2832528817

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561755_139561756insTCTTCCACAGTGG , CM000685.2:g.139561755_139561756insTCTTCCACAGTGG	GRCh38
NC_000023.10:g.138643914_138643915insTCTTCCACAGTGG , CM000685.1:g.138643914_138643915insTCTTCCACAGTGG	GRCh37
NC_000023.9:g.138471580_138471581insTCTTCCACAGTGG	NCBI36
NG_007994.1:g.36020_36021insTCTTCCACAGTGG , LRG_556:g.36020_36021insTCTTCCACAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1070_1071insTCTTCCACAGTGG MANE Select	ENSP00000218099.2:p.Arg358LeufsTer20
ENST00000643157.1:n.1723+14_1723+15insTCTTCCACAGTGG
ENST00000218099.6:c.1070_1071insTCTTCCACAGTGG	ENSP00000218099.2:p.Arg358LeufsTer20
ENST00000394090.2:c.956_957insTCTTCCACAGTGG	ENSP00000377650.2:p.Arg320LeufsTer20
NM_000133.3:c.1070_1071insTCTTCCACAGTGG , LRG_556t1:c.1070_1071insTCTTCCACAGTGG	NP_000124.1:p.Arg358LeufsTer20
NM_001313913.1:c.956_957insTCTTCCACAGTGG	NP_001300842.1:p.Arg320LeufsTer20
XM_005262397.3:c.941_942insTCTTCCACAGTGG	XP_005262454.1:p.Arg315LeufsTer20
XM_005262397.4:c.941_942insTCTTCCACAGTGG	XP_005262454.1:p.Arg315LeufsTer20
NM_000133.4:c.1070_1071insTCTTCCACAGTGG MANE Select	NP_000124.1:p.Arg358LeufsTer20
NM_001313913.2:c.956_957insTCTTCCACAGTGG	NP_001300842.1:p.Arg320LeufsTer20