Canonical Allele Identifier: CA112105780

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs796075226

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288071_186288075delinsACATCT , CM000666.2:g.186288071_186288075delinsACATCT	GRCh38
NC_000004.11:g.187209225_187209229delinsACATCT , CM000666.1:g.187209225_187209229delinsACATCT	GRCh37
NC_000004.10:g.187446219_187446223delinsACATCT	NCBI36
NG_008051.1:g.27108_27112delinsACATCT , LRG_583:g.27108_27112delinsACATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+248_1716+252delinsACATCT (F11) MANE Select	ENSP00000384957.2:n.1716+248_1716+252delinsACATCT
ENST00000264691.4:c.316+248_316+252delinsACATCT (F11)
ENST00000264692.8:c.1554+248_1554+252delinsACATCT (F11)	ENSP00000264692.5:n.1554+248_1554+252delinsACATCT
ENST00000403665.6:c.1716+248_1716+252delinsACATCT (F11)	ENSP00000384957.2:n.1716+248_1716+252delinsACATCT
ENST00000503841.1:n.235+248_235+252delinsACATCT (F11)
NM_000128.3:c.1716+248_1716+252delinsACATCT , LRG_583t1:c.1716+248_1716+252delinsACATCT (F11)	NP_000119.1:n.1716+248_1716+252delinsACATCT
NR_033900.1:n.1066+353_1066+357delinsAGATGT (F11-AS1)
XM_005262821.2:c.1719+248_1719+252delinsACATCT (F11)	XP_005262878.1:n.1719+248_1719+252delinsACATCT
XM_005262822.2:c.1623+248_1623+252delinsACATCT (F11)	XP_005262879.1:n.1623+248_1623+252delinsACATCT
XM_005262823.2:c.1449+248_1449+252delinsACATCT (F11)	XP_005262880.1:n.1449+248_1449+252delinsACATCT
XM_006714137.1:c.1671+248_1671+252delinsACATCT (F11)	XP_006714200.1:n.1671+248_1671+252delinsACATCT
XM_005262821.4:c.1719+248_1719+252delinsACATCT (F11)	XP_005262878.1:n.1719+248_1719+252delinsACATCT
XM_005262822.4:c.1623+248_1623+252delinsACATCT (F11)	XP_005262879.1:n.1623+248_1623+252delinsACATCT
XM_005262823.4:c.1449+248_1449+252delinsACATCT (F11)	XP_005262880.1:n.1449+248_1449+252delinsACATCT
XM_006714137.3:c.1671+248_1671+252delinsACATCT (F11)	XP_006714200.1:n.1671+248_1671+252delinsACATCT
NM_000128.4:c.1716+248_1716+252delinsACATCT (F11) MANE Select	NP_000119.1:n.1716+248_1716+252delinsACATCT