Canonical Allele Identifier: CA255375

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561683C>T , CM000685.2:g.139561683C>T	GRCh38
NC_000023.10:g.138643842C>T , CM000685.1:g.138643842C>T	GRCh37
NC_000023.9:g.138471508C>T	NCBI36
NG_007994.1:g.35948C>T , LRG_556:g.35948C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.998C>T MANE Select	ENSP00000218099.2:p.Pro333Leu
ENST00000643157.1:n.1665C>T
ENST00000218099.6:c.998C>T	ENSP00000218099.2:p.Pro333Leu
ENST00000394090.2:c.884C>T	ENSP00000377650.2:p.Pro295Leu
NM_000133.3:c.998C>T , LRG_556t1:c.998C>T	NP_000124.1:p.Pro333Leu
NM_001313913.1:c.884C>T	NP_001300842.1:p.Pro295Leu
XM_005262397.3:c.869C>T	XP_005262454.1:p.Pro290Leu
XM_005262397.4:c.869C>T	XP_005262454.1:p.Pro290Leu
NM_000133.4:c.998C>T MANE Select	NP_000124.1:p.Pro333Leu
NM_001313913.2:c.884C>T	NP_001300842.1:p.Pro295Leu