Canonical Allele Identifier: CA1969072667

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726507_46726510delinsTGGA , CM000673.2:g.46726507_46726510delinsTGGA	GRCh38
NC_000011.9:g.46748057_46748060delinsTGGA , CM000673.1:g.46748057_46748060delinsTGGA	GRCh37
NC_000011.8:g.46704633_46704636delinsTGGA	NCBI36
NG_008953.1:g.12315_12318delinsTGGA , LRG_551:g.12315_12318delinsTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.884_887delinsTGGA MANE Select	ENSP00000308541.5:p.Val295=
ENST00000311907.9:c.884_887delinsTGGA	ENSP00000308541.5:p.Val295=
ENST00000442468.1:c.854_857delinsTGGA	ENSP00000387413.1:p.Val285=
ENST00000530231.5:c.884_887delinsTGGA	ENSP00000433907.1:p.Val295=
NM_000506.3:c.884_887delinsTGGA	NP_000497.1:p.Val295=
NM_000506.4:c.884_887delinsTGGA , LRG_551t1:c.884_887delinsTGGA	NP_000497.1:p.Val295=
NM_001311257.1:c.836_839delinsTGGA	NP_001298186.1:p.Val279=
XR_428840.2:n.928_931delinsTGGA
XR_428840.4:n.919_922delinsTGGA
NM_000506.5:c.884_887delinsTGGA MANE Select	NP_000497.1:p.Val295=
NM_001311257.2:c.836_839delinsTGGA	NP_001298186.1:p.Val279=