Canonical Allele Identifier: CA414444829

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643775A>C (hg19) ; chrX:g.139561616A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561616A>C , CM000685.2:g.139561616A>C	GRCh38
NC_000023.10:g.138643775A>C , CM000685.1:g.138643775A>C	GRCh37
NC_000023.9:g.138471441A>C	NCBI36
NG_007994.1:g.35881A>C , LRG_556:g.35881A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.931A>C MANE Select	ENSP00000218099.2:p.Lys311Gln
ENST00000643157.1:n.1598A>C
ENST00000218099.6:c.931A>C	ENSP00000218099.2:p.Lys311Gln
ENST00000394090.2:c.817A>C	ENSP00000377650.2:p.Lys273Gln
NM_000133.3:c.931A>C , LRG_556t1:c.931A>C	NP_000124.1:p.Lys311Gln
NM_001313913.1:c.817A>C	NP_001300842.1:p.Lys273Gln
XM_005262397.3:c.802A>C	XP_005262454.1:p.Lys268Gln
XM_005262397.4:c.802A>C	XP_005262454.1:p.Lys268Gln
NM_000133.4:c.931A>C MANE Select	NP_000124.1:p.Lys311Gln
NM_001313913.2:c.817A>C	NP_001300842.1:p.Lys273Gln