Canonical Allele Identifier: CA918871544

Gene: F2

Linked Data

• dbSNP Id: rs1592414084

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727845_46727861del , CM000673.2:g.46727845_46727861del	GRCh38
NC_000011.9:g.46749395_46749411del , CM000673.1:g.46749395_46749411del	GRCh37
NC_000011.8:g.46705971_46705987del	NCBI36
NG_008953.1:g.13653_13669del , LRG_551:g.13653_13669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-151_1131-135del MANE Select	ENSP00000308541.5:n.1131-151_1131-135del
ENST00000311907.9:c.1131-151_1131-135del	ENSP00000308541.5:n.1131-151_1131-135del
ENST00000530231.5:c.1131-151_1131-135del	ENSP00000433907.1:n.1131-151_1131-135del
NM_000506.3:c.1131-151_1131-135del	NP_000497.1:n.1131-151_1131-135del
NM_000506.4:c.1131-151_1131-135del , LRG_551t1:c.1131-151_1131-135del	NP_000497.1:n.1131-151_1131-135del
NM_001311257.1:c.1083-151_1083-135del	NP_001298186.1:n.1083-151_1083-135del
XR_428840.2:n.1175-151_1175-135del
XR_428840.4:n.1166-151_1166-135del
NM_000506.5:c.1131-151_1131-135del MANE Select	NP_000497.1:n.1131-151_1131-135del
NM_001311257.2:c.1083-151_1083-135del	NP_001298186.1:n.1083-151_1083-135del