Canonical Allele Identifier: CA2695236388

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561915_139561916delinsCG , CM000685.2:g.139561915_139561916delinsCG	GRCh38
NC_000023.10:g.138644074_138644075delinsCG , CM000685.1:g.138644074_138644075delinsCG	GRCh37
NC_000023.9:g.138471740_138471741delinsCG	NCBI36
NG_007994.1:g.36180_36181delinsCG , LRG_556:g.36180_36181delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1230_1231delinsCG MANE Select	ENSP00000218099.2:p.Ser411Gly
ENST00000643157.1:n.1723+174_1723+175delinsCG
ENST00000218099.6:c.1230_1231delinsCG	ENSP00000218099.2:p.Ser411Gly
ENST00000394090.2:c.1116_1117delinsCG	ENSP00000377650.2:p.Ser373Gly
NM_000133.3:c.1230_1231delinsCG , LRG_556t1:c.1230_1231delinsCG	NP_000124.1:p.Ser411Gly
NM_001313913.1:c.1116_1117delinsCG	NP_001300842.1:p.Ser373Gly
XM_005262397.3:c.1101_1102delinsCG	XP_005262454.1:p.Ser368Gly
XM_005262397.4:c.1101_1102delinsCG	XP_005262454.1:p.Ser368Gly
NM_000133.4:c.1230_1231delinsCG MANE Select	NP_000124.1:p.Ser411Gly
NM_001313913.2:c.1116_1117delinsCG	NP_001300842.1:p.Ser373Gly