Canonical Allele Identifier: CA792317134

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1228145053
• gnomAD v3: 4-186287899-TG-T
• gnomAD v4: 4-186287899-TG-T
• MyVariant Identifiers: chr4:g.187209054del (hg19) ; chr4:g.186287900del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287900del , CM000666.2:g.186287900del	GRCh38
NC_000004.11:g.187209054del , CM000666.1:g.187209054del	GRCh37
NC_000004.10:g.187446048del	NCBI36
NG_008051.1:g.26937del , LRG_583:g.26937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+77del (F11) MANE Select	ENSP00000384957.2:n.1716+77del
ENST00000264691.4:c.316+77del (F11)
ENST00000264692.8:c.1554+77del (F11)	ENSP00000264692.5:n.1554+77del
ENST00000403665.6:c.1716+77del (F11)	ENSP00000384957.2:n.1716+77del
ENST00000503841.1:n.235+77del (F11)
NM_000128.3:c.1716+77del , LRG_583t1:c.1716+77del (F11)	NP_000119.1:n.1716+77del
NR_033900.1:n.1066+528del (F11-AS1)
XM_005262821.2:c.1719+77del (F11)	XP_005262878.1:n.1719+77del
XM_005262822.2:c.1623+77del (F11)	XP_005262879.1:n.1623+77del
XM_005262823.2:c.1449+77del (F11)	XP_005262880.1:n.1449+77del
XM_006714137.1:c.1671+77del (F11)	XP_006714200.1:n.1671+77del
XM_005262821.4:c.1719+77del (F11)	XP_005262878.1:n.1719+77del
XM_005262822.4:c.1623+77del (F11)	XP_005262879.1:n.1623+77del
XM_005262823.4:c.1449+77del (F11)	XP_005262880.1:n.1449+77del
XM_006714137.3:c.1671+77del (F11)	XP_006714200.1:n.1671+77del
NM_000128.4:c.1716+77del (F11) MANE Select	NP_000119.1:n.1716+77del