Canonical Allele Identifier: CA1969073859

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727901_46727909delinsGCTGGGTTC , CM000673.2:g.46727901_46727909delinsGCTGGGTTC	GRCh38
NC_000011.9:g.46749451_46749459delinsGCTGGGTTC , CM000673.1:g.46749451_46749459delinsGCTGGGTTC	GRCh37
NC_000011.8:g.46706027_46706035delinsGCTGGGTTC	NCBI36
NG_008953.1:g.13709_13717delinsGCTGGGTTC , LRG_551:g.13709_13717delinsGCTGGGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-95_1131-87delinsGCTGGGTTC MANE Select	ENSP00000308541.5:n.1131-95_1131-87delinsGCTGGGTTC
ENST00000311907.9:c.1131-95_1131-87delinsGCTGGGTTC	ENSP00000308541.5:n.1131-95_1131-87delinsGCTGGGTTC
ENST00000530231.5:c.1131-95_1131-87delinsGCTGGGTTC	ENSP00000433907.1:n.1131-95_1131-87delinsGCTGGGTTC
NM_000506.3:c.1131-95_1131-87delinsGCTGGGTTC	NP_000497.1:n.1131-95_1131-87delinsGCTGGGTTC
NM_000506.4:c.1131-95_1131-87delinsGCTGGGTTC , LRG_551t1:c.1131-95_1131-87delinsGCTGGGTTC	NP_000497.1:n.1131-95_1131-87delinsGCTGGGTTC
NM_001311257.1:c.1083-95_1083-87delinsGCTGGGTTC	NP_001298186.1:n.1083-95_1083-87delinsGCTGGGTTC
XR_428840.2:n.1175-95_1175-87delinsGCTGGGTTC
XR_428840.4:n.1166-95_1166-87delinsGCTGGGTTC
NM_000506.5:c.1131-95_1131-87delinsGCTGGGTTC MANE Select	NP_000497.1:n.1131-95_1131-87delinsGCTGGGTTC
NM_001311257.2:c.1083-95_1083-87delinsGCTGGGTTC	NP_001298186.1:n.1083-95_1083-87delinsGCTGGGTTC