Canonical Allele Identifier: CA221652424

Gene: F2

Linked Data

• dbSNP Id: rs147747444
• MyVariant Identifiers: chr11:g.46747781_46747782insCCC (hg19) ; chr11:g.46726231_46726232insCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726232_46726233insCCC , CM000673.2:g.46726232_46726233insCCC	GRCh38
NC_000011.9:g.46747782_46747783insCCC , CM000673.1:g.46747782_46747783insCCC	GRCh37
NC_000011.8:g.46704358_46704359insCCC	NCBI36
NG_008953.1:g.12040_12041insCCC , LRG_551:g.12040_12041insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+59_874+60insCCC MANE Select	ENSP00000308541.5:n.874+59_874+60insCCC
ENST00000311907.9:c.874+59_874+60insCCC	ENSP00000308541.5:n.874+59_874+60insCCC
ENST00000442468.1:c.844+59_844+60insCCC	ENSP00000387413.1:n.844+59_844+60insCCC
ENST00000530231.5:c.874+59_874+60insCCC	ENSP00000433907.1:n.874+59_874+60insCCC
NM_000506.3:c.874+59_874+60insCCC	NP_000497.1:n.874+59_874+60insCCC
NM_000506.4:c.874+59_874+60insCCC , LRG_551t1:c.874+59_874+60insCCC	NP_000497.1:n.874+59_874+60insCCC
NM_001311257.1:c.826+59_826+60insCCC	NP_001298186.1:n.826+59_826+60insCCC
XR_428840.2:n.918+59_918+60insCCC
XR_428840.4:n.909+59_909+60insCCC
NM_000506.5:c.874+59_874+60insCCC MANE Select	NP_000497.1:n.874+59_874+60insCCC
NM_001311257.2:c.826+59_826+60insCCC	NP_001298186.1:n.826+59_826+60insCCC