Canonical Allele Identifier: CA557396163

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1246159495
• gnomAD v2: 4-187209982-CTT-C
• gnomAD v4: 4-186288828-CTT-C
• MyVariant Identifiers: chr4:g.187209983_187209984del (hg19) ; chr4:g.186288829_186288830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288830_186288831del , CM000666.2:g.186288830_186288831del	GRCh38
NC_000004.11:g.187209984_187209985del , CM000666.1:g.187209984_187209985del	GRCh37
NC_000004.10:g.187446978_187446979del	NCBI36
NG_008051.1:g.27867_27868del , LRG_583:g.27867_27868del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*216_*217del (F11) MANE Select	ENSP00000384957.2:n.*216_*217del
NM_000128.3:c.*216_*217del , LRG_583t1:c.*216_*217del (F11)	NP_000119.1:n.*216_*217del
NR_033900.1:n.664_665del (F11-AS1)
XM_005262821.2:c.*216_*217del (F11)	XP_005262878.1:n.*216_*217del
XM_005262822.2:c.*216_*217del (F11)	XP_005262879.1:n.*216_*217del
XM_005262823.2:c.*216_*217del (F11)	XP_005262880.1:n.*216_*217del
XM_006714137.1:c.*216_*217del (F11)	XP_006714200.1:n.*216_*217del
XM_005262821.4:c.*216_*217del (F11)	XP_005262878.1:n.*216_*217del
XM_005262822.4:c.*216_*217del (F11)	XP_005262879.1:n.*216_*217del
XM_005262823.4:c.*216_*217del (F11)	XP_005262880.1:n.*216_*217del
XM_006714137.3:c.*216_*217del (F11)	XP_006714200.1:n.*216_*217del
NM_000128.4:c.*216_*217del (F11) MANE Select	NP_000119.1:n.*216_*217del