Canonical Allele Identifier: CA2672904209

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288853-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288853_186288854insC , CM000666.2:g.186288853_186288854insC	GRCh38
NC_000004.11:g.187210007_187210008insC , CM000666.1:g.187210007_187210008insC	GRCh37
NC_000004.10:g.187447001_187447002insC	NCBI36
NG_008051.1:g.27890_27891insC , LRG_583:g.27890_27891insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*239_*240insC (F11) MANE Select	ENSP00000384957.2:n.*239_*240insC
NM_000128.3:c.*239_*240insC , LRG_583t1:c.*239_*240insC (F11)	NP_000119.1:n.*239_*240insC
NR_033900.1:n.640_641insG (F11-AS1)
XM_005262821.2:c.*239_*240insC (F11)	XP_005262878.1:n.*239_*240insC
XM_005262822.2:c.*239_*240insC (F11)	XP_005262879.1:n.*239_*240insC
XM_005262823.2:c.*239_*240insC (F11)	XP_005262880.1:n.*239_*240insC
XM_006714137.1:c.*239_*240insC (F11)	XP_006714200.1:n.*239_*240insC
XM_005262821.4:c.*239_*240insC (F11)	XP_005262878.1:n.*239_*240insC
XM_005262822.4:c.*239_*240insC (F11)	XP_005262879.1:n.*239_*240insC
XM_005262823.4:c.*239_*240insC (F11)	XP_005262880.1:n.*239_*240insC
XM_006714137.3:c.*239_*240insC (F11)	XP_006714200.1:n.*239_*240insC
NM_000128.4:c.*239_*240insC (F11) MANE Select	NP_000119.1:n.*239_*240insC