Canonical Allele Identifier: CA3163527

Gene: F11

Linked Data

• dbSNP Id: rs745753344
• ExAC: 4:187188257 GT / G
• gnomAD v2: 4-187188257-GT-G
• gnomAD v4: 4-186267103-GT-G
• MyVariant Identifiers: chr4:g.187188258del (hg19) ; chr4:g.186267104del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186267105del , CM000666.2:g.186267105del	GRCh38
NC_000004.11:g.187188259del , CM000666.1:g.187188259del	GRCh37
NC_000004.10:g.187425253del	NCBI36
NG_008051.1:g.6142del , LRG_583:g.6142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-1-31del MANE Select	ENSP00000384957.2:n.-1-31del
ENST00000264692.8:c.-1-31del	ENSP00000264692.5:n.-1-31del
ENST00000403665.6:c.-1-31del	ENSP00000384957.2:n.-1-31del
ENST00000492972.6:c.-1-31del	ENSP00000424479.1:n.-1-31del
NM_000128.3:c.-1-31del , LRG_583t1:c.-1-31del	NP_000119.1:n.-1-31del
XM_005262821.2:c.-1-31del	XP_005262878.1:n.-1-31del
XM_005262822.2:c.-1-31del	XP_005262879.1:n.-1-31del
XM_005262823.2:c.-1-31del	XP_005262880.1:n.-1-31del
XM_005262824.1:c.-1-31del	XP_005262881.1:n.-1-31del
XM_006714137.1:c.-1-31del	XP_006714200.1:n.-1-31del
XR_938706.1:n.352-31del
XR_938707.1:n.352-31del
NM_001354804.1:c.-1-31del	NP_001341733.1:n.-1-31del
XM_005262821.4:c.-1-31del	XP_005262878.1:n.-1-31del
XM_005262822.4:c.-1-31del	XP_005262879.1:n.-1-31del
XM_005262823.4:c.-1-31del	XP_005262880.1:n.-1-31del
XM_006714137.3:c.-1-31del	XP_006714200.1:n.-1-31del
XM_017007884.2:c.-1-31del	XP_016863373.1:n.-1-31del
XM_017007885.2:c.-1-31del	XP_016863374.1:n.-1-31del
XM_017007886.2:c.-1-31del	XP_016863375.1:n.-1-31del
XR_001741172.2:n.333-31del
NM_000128.4:c.-1-31del MANE Select	NP_000119.1:n.-1-31del
NM_001354804.2:c.-1-31del	NP_001341733.1:n.-1-31del