Canonical Allele Identifier: CA645571956

Gene: F2

Linked Data

• COSMIC: COSM1703855

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726098_46726099delinsAA , CM000673.2:g.46726098_46726099delinsAA	GRCh38
NC_000011.9:g.46747648_46747649delinsAA , CM000673.1:g.46747648_46747649delinsAA	GRCh37
NC_000011.8:g.46704224_46704225delinsAA	NCBI36
NG_008953.1:g.11906_11907delinsAA , LRG_551:g.11906_11907delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.799_800delinsAA MANE Select	ENSP00000308541.5:p.Gly267Lys
ENST00000311907.9:c.799_800delinsAA	ENSP00000308541.5:p.Gly267Lys
ENST00000442468.1:c.769_770delinsAA	ENSP00000387413.1:p.Gly257Lys
ENST00000530231.5:c.799_800delinsAA	ENSP00000433907.1:p.Gly267Lys
NM_000506.3:c.799_800delinsAA	NP_000497.1:p.Gly267Lys
NM_000506.4:c.799_800delinsAA , LRG_551t1:c.799_800delinsAA	NP_000497.1:p.Gly267Lys
NM_001311257.1:c.751_752delinsAA	NP_001298186.1:p.Gly251Lys
XR_428840.2:n.843_844delinsAA
XR_428840.4:n.834_835delinsAA
NM_000506.5:c.799_800delinsAA MANE Select	NP_000497.1:p.Gly267Lys
NM_001311257.2:c.751_752delinsAA	NP_001298186.1:p.Gly251Lys