Canonical Allele Identifier: CA1519935942

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280185_186280187delinsAGG , CM000666.2:g.186280185_186280187delinsAGG	GRCh38
NC_000004.11:g.187201339_187201341delinsAGG , CM000666.1:g.187201339_187201341delinsAGG	GRCh37
NC_000004.10:g.187438333_187438335delinsAGG	NCBI36
NG_008051.1:g.19222_19224delinsAGG , LRG_583:g.19222_19224delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.866-38_866-36delinsAGG MANE Select	ENSP00000384957.2:n.866-38_866-36delinsAGG
ENST00000264692.8:c.704-38_704-36delinsAGG	ENSP00000264692.5:n.704-38_704-36delinsAGG
ENST00000403665.6:c.866-38_866-36delinsAGG	ENSP00000384957.2:n.866-38_866-36delinsAGG
ENST00000452239.1:c.313-38_313-36delinsAGG
NM_000128.3:c.866-38_866-36delinsAGG , LRG_583t1:c.866-38_866-36delinsAGG	NP_000119.1:n.866-38_866-36delinsAGG
XM_005262821.2:c.866-38_866-36delinsAGG	XP_005262878.1:n.866-38_866-36delinsAGG
XM_005262822.2:c.866-38_866-36delinsAGG	XP_005262879.1:n.866-38_866-36delinsAGG
XM_005262823.2:c.596-38_596-36delinsAGG	XP_005262880.1:n.596-38_596-36delinsAGG
XM_005262824.1:c.866-38_866-36delinsAGG	XP_005262881.1:n.866-38_866-36delinsAGG
XM_006714137.1:c.865+64_865+66delinsAGG	XP_006714200.1:n.865+64_865+66delinsAGG
XR_938706.1:n.1218-38_1218-36delinsAGG
XR_938707.1:n.1218-38_1218-36delinsAGG
XM_005262821.4:c.866-38_866-36delinsAGG	XP_005262878.1:n.866-38_866-36delinsAGG
XM_005262822.4:c.866-38_866-36delinsAGG	XP_005262879.1:n.866-38_866-36delinsAGG
XM_005262823.4:c.596-38_596-36delinsAGG	XP_005262880.1:n.596-38_596-36delinsAGG
XM_006714137.3:c.865+64_865+66delinsAGG	XP_006714200.1:n.865+64_865+66delinsAGG
XM_017007884.2:c.866-38_866-36delinsAGG	XP_016863373.1:n.866-38_866-36delinsAGG
XM_017007885.2:c.866-38_866-36delinsAGG	XP_016863374.1:n.866-38_866-36delinsAGG
XM_017007886.2:c.866-38_866-36delinsAGG	XP_016863375.1:n.866-38_866-36delinsAGG
XR_001741172.2:n.1199-38_1199-36delinsAGG
NM_000128.4:c.866-38_866-36delinsAGG MANE Select	NP_000119.1:n.866-38_866-36delinsAGG