Canonical Allele Identifier: CA2499740608

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561804_139561805insAG , CM000685.2:g.139561804_139561805insAG	GRCh38
NC_000023.10:g.138643963_138643964insAG , CM000685.1:g.138643963_138643964insAG	GRCh37
NC_000023.9:g.138471629_138471630insAG	NCBI36
NG_007994.1:g.36069_36070insAG , LRG_556:g.36069_36070insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1119_1120insAG MANE Select	ENSP00000218099.2:p.Val374ArgfsTer?
ENST00000643157.1:n.1723+63_1723+64insAG
ENST00000218099.6:c.1119_1120insAG	ENSP00000218099.2:p.Val374ArgfsTer?
ENST00000394090.2:c.1005_1006insAG	ENSP00000377650.2:p.Val336ArgfsTer?
NM_000133.3:c.1119_1120insAG , LRG_556t1:c.1119_1120insAG	NP_000124.1:p.Val374ArgfsTer?
NM_001313913.1:c.1005_1006insAG	NP_001300842.1:p.Val336ArgfsTer?
XM_005262397.3:c.990_991insAG	XP_005262454.1:p.Val331ArgfsTer?
XM_005262397.4:c.990_991insAG	XP_005262454.1:p.Val331ArgfsTer?
NM_000133.4:c.1119_1120insAG MANE Select	NP_000124.1:p.Val374ArgfsTer?
NM_001313913.2:c.1005_1006insAG	NP_001300842.1:p.Val336ArgfsTer?