Canonical Allele Identifier: CA414437961

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541182T>A , CM000685.2:g.139541182T>A	GRCh38
NC_000023.10:g.138623341T>A , CM000685.1:g.138623341T>A	GRCh37
NC_000023.9:g.138451007T>A	NCBI36
NG_007994.1:g.15447T>A , LRG_556:g.15447T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.384T>A MANE Select	ENSP00000218099.2:p.Cys128Ter
ENST00000218099.6:c.384T>A	ENSP00000218099.2:p.Cys128Ter
ENST00000394090.2:c.277+3796T>A	ENSP00000377650.2:n.277+3796T>A
ENST00000479617.2:n.337T>A
NM_000133.3:c.384T>A , LRG_556t1:c.384T>A	NP_000124.1:p.Cys128Ter
NM_001313913.1:c.277+3796T>A	NP_001300842.1:n.277+3796T>A
XM_005262397.3:c.384T>A	XP_005262454.1:p.Cys128Ter
XM_005262397.4:c.384T>A	XP_005262454.1:p.Cys128Ter
NM_000133.4:c.384T>A MANE Select	NP_000124.1:p.Cys128Ter
NM_001313913.2:c.277+3796T>A	NP_001300842.1:n.277+3796T>A