Canonical Allele Identifier: CA518916514

Gene: F9

Linked Data

• gnomAD v4: X-139561618-G-A
• MyVariant Identifiers: chrX:g.138643777G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561618G>A , CM000685.2:g.139561618G>A	GRCh38
NC_000023.10:g.138643777G>A , CM000685.1:g.138643777G>A	GRCh37
NC_000023.9:g.138471443G>A	NCBI36
NG_007994.1:g.35883G>A , LRG_556:g.35883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.933G>A MANE Select	ENSP00000218099.2:p.Lys311=
ENST00000643157.1:n.1600G>A
ENST00000218099.6:c.933G>A	ENSP00000218099.2:p.Lys311=
ENST00000394090.2:c.819G>A	ENSP00000377650.2:p.Lys273=
NM_000133.3:c.933G>A , LRG_556t1:c.933G>A	NP_000124.1:p.Lys311=
NM_001313913.1:c.819G>A	NP_001300842.1:p.Lys273=
XM_005262397.3:c.804G>A	XP_005262454.1:p.Lys268=
XM_005262397.4:c.804G>A	XP_005262454.1:p.Lys268=
NM_000133.4:c.933G>A MANE Select	NP_000124.1:p.Lys311=
NM_001313913.2:c.819G>A	NP_001300842.1:p.Lys273=