Canonical Allele Identifier: CA1519939954

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288826_186288830delinsCTCTT , CM000666.2:g.186288826_186288830delinsCTCTT	GRCh38
NC_000004.11:g.187209980_187209984delinsCTCTT , CM000666.1:g.187209980_187209984delinsCTCTT	GRCh37
NC_000004.10:g.187446974_187446978delinsCTCTT	NCBI36
NG_008051.1:g.27863_27867delinsCTCTT , LRG_583:g.27863_27867delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*212_*216delinsCTCTT (F11) MANE Select	ENSP00000384957.2:n.*212_*216delinsCTCTT
NM_000128.3:c.*212_*216delinsCTCTT , LRG_583t1:c.*212_*216delinsCTCTT (F11)	NP_000119.1:n.*212_*216delinsCTCTT
NR_033900.1:n.664_668delinsAAGAG (F11-AS1)
XM_005262821.2:c.*212_*216delinsCTCTT (F11)	XP_005262878.1:n.*212_*216delinsCTCTT
XM_005262822.2:c.*212_*216delinsCTCTT (F11)	XP_005262879.1:n.*212_*216delinsCTCTT
XM_005262823.2:c.*212_*216delinsCTCTT (F11)	XP_005262880.1:n.*212_*216delinsCTCTT
XM_006714137.1:c.*212_*216delinsCTCTT (F11)	XP_006714200.1:n.*212_*216delinsCTCTT
XM_005262821.4:c.*212_*216delinsCTCTT (F11)	XP_005262878.1:n.*212_*216delinsCTCTT
XM_005262822.4:c.*212_*216delinsCTCTT (F11)	XP_005262879.1:n.*212_*216delinsCTCTT
XM_005262823.4:c.*212_*216delinsCTCTT (F11)	XP_005262880.1:n.*212_*216delinsCTCTT
XM_006714137.3:c.*212_*216delinsCTCTT (F11)	XP_006714200.1:n.*212_*216delinsCTCTT
NM_000128.4:c.*212_*216delinsCTCTT (F11) MANE Select	NP_000119.1:n.*212_*216delinsCTCTT