Canonical Allele Identifier: CA414447577
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562050G>T , CM000685.2:g.139562050G>T GRCh38
NC_000023.10:g.138644209G>T , CM000685.1:g.138644209G>T GRCh37
NC_000023.9:g.138471875G>T NCBI36
NG_007994.1:g.36315G>T , LRG_556:g.36315G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1365G>T MANE Select ENSP00000218099.2:p.Lys455Asn
ENST00000643157.1:n.1723+309G>T
ENST00000218099.6:c.1365G>T ENSP00000218099.2:p.Lys455Asn
ENST00000394090.2:c.1251G>T ENSP00000377650.2:p.Lys417Asn
NM_000133.3:c.1365G>T , LRG_556t1:c.1365G>T NP_000124.1:p.Lys455Asn
NM_001313913.1:c.1251G>T NP_001300842.1:p.Lys417Asn
XM_005262397.3:c.1236G>T XP_005262454.1:p.Lys412Asn
XM_005262397.4:c.1236G>T XP_005262454.1:p.Lys412Asn
NM_000133.4:c.1365G>T MANE Select NP_000124.1:p.Lys455Asn
NM_001313913.2:c.1251G>T NP_001300842.1:p.Lys417Asn