Canonical Allele Identifier: CA1969071891

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725861_46725877delinsCAGGATCAAGTCACTGT , CM000673.2:g.46725861_46725877delinsCAGGATCAAGTCACTGT	GRCh38
NC_000011.9:g.46747411_46747427delinsCAGGATCAAGTCACTGT , CM000673.1:g.46747411_46747427delinsCAGGATCAAGTCACTGT	GRCh37
NC_000011.8:g.46703987_46704003delinsCAGGATCAAGTCACTGT	NCBI36
NG_008953.1:g.11669_11685delinsCAGGATCAAGTCACTGT , LRG_551:g.11669_11685delinsCAGGATCAAGTCACTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.562_578delinsCAGGATCAAGTCACTGT MANE Select	ENSP00000308541.5:p.Gln188=
ENST00000311907.9:c.562_578delinsCAGGATCAAGTCACTGT	ENSP00000308541.5:p.Gln188=
ENST00000442468.1:c.532_548delinsCAGGATCAAGTCACTGT	ENSP00000387413.1:p.Gln178=
ENST00000490274.1:n.342_358delinsCAGGATCAAGTCACTGT
ENST00000530231.5:c.562_578delinsCAGGATCAAGTCACTGT	ENSP00000433907.1:p.Gln188=
NM_000506.3:c.562_578delinsCAGGATCAAGTCACTGT	NP_000497.1:p.Gln188=
NM_000506.4:c.562_578delinsCAGGATCAAGTCACTGT , LRG_551t1:c.562_578delinsCAGGATCAAGTCACTGT	NP_000497.1:p.Gln188=
NM_001311257.1:c.514_530delinsCAGGATCAAGTCACTGT	NP_001298186.1:p.Gln172=
XR_428840.2:n.606_622delinsCAGGATCAAGTCACTGT
XR_428840.4:n.597_613delinsCAGGATCAAGTCACTGT
NM_000506.5:c.562_578delinsCAGGATCAAGTCACTGT MANE Select	NP_000497.1:p.Gln188=
NM_001311257.2:c.514_530delinsCAGGATCAAGTCACTGT	NP_001298186.1:p.Gln172=