Canonical Allele Identifier: CA2574810795

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725964del , CM000673.2:g.46725964del	GRCh38
NC_000011.9:g.46747514del , CM000673.1:g.46747514del	GRCh37
NC_000011.8:g.46704090del	NCBI36
NG_008953.1:g.11772del , LRG_551:g.11772del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.665del MANE Select	ENSP00000308541.5:p.Gln222ArgfsTer6
ENST00000311907.9:c.665del	ENSP00000308541.5:p.Gln222ArgfsTer6
ENST00000442468.1:c.635del	ENSP00000387413.1:p.Gln212ArgfsTer6
ENST00000490274.1:n.445del
ENST00000530231.5:c.665del	ENSP00000433907.1:p.Gln222ArgfsTer6
NM_000506.3:c.665del	NP_000497.1:p.Gln222ArgfsTer6
NM_000506.4:c.665del , LRG_551t1:c.665del	NP_000497.1:p.Gln222ArgfsTer6
NM_001311257.1:c.617del	NP_001298186.1:p.Gln206ArgfsTer6
XR_428840.2:n.709del
XR_428840.4:n.700del
NM_000506.5:c.665del MANE Select	NP_000497.1:p.Gln222ArgfsTer6
NM_001311257.2:c.617del	NP_001298186.1:p.Gln206ArgfsTer6