Canonical Allele Identifier: CA2695204103

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280124_186280134del , CM000666.2:g.186280124_186280134del	GRCh38
NC_000004.11:g.187201278_187201288del , CM000666.1:g.187201278_187201288del	GRCh37
NC_000004.10:g.187438272_187438282del	NCBI36
NG_008051.1:g.19161_19171del , LRG_583:g.19161_19171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.865+3_865+13del MANE Select	ENSP00000384957.2:n.865+3_865+13del
ENST00000264692.8:c.703+3_703+13del	ENSP00000264692.5:n.703+3_703+13del
ENST00000403665.6:c.865+3_865+13del	ENSP00000384957.2:n.865+3_865+13del
ENST00000452239.1:c.312+3_312+13del
NM_000128.3:c.865+3_865+13del , LRG_583t1:c.865+3_865+13del	NP_000119.1:n.865+3_865+13del
XM_005262821.2:c.865+3_865+13del	XP_005262878.1:n.865+3_865+13del
XM_005262822.2:c.865+3_865+13del	XP_005262879.1:n.865+3_865+13del
XM_005262823.2:c.595+3_595+13del	XP_005262880.1:n.595+3_595+13del
XM_005262824.1:c.865+3_865+13del	XP_005262881.1:n.865+3_865+13del
XM_006714137.1:c.865+3_865+13del	XP_006714200.1:n.865+3_865+13del
XR_938706.1:n.1217+3_1217+13del
XR_938707.1:n.1217+3_1217+13del
XM_005262821.4:c.865+3_865+13del	XP_005262878.1:n.865+3_865+13del
XM_005262822.4:c.865+3_865+13del	XP_005262879.1:n.865+3_865+13del
XM_005262823.4:c.595+3_595+13del	XP_005262880.1:n.595+3_595+13del
XM_006714137.3:c.865+3_865+13del	XP_006714200.1:n.865+3_865+13del
XM_017007884.2:c.865+3_865+13del	XP_016863373.1:n.865+3_865+13del
XM_017007885.2:c.865+3_865+13del	XP_016863374.1:n.865+3_865+13del
XM_017007886.2:c.865+3_865+13del	XP_016863375.1:n.865+3_865+13del
XR_001741172.2:n.1198+3_1198+13del
NM_000128.4:c.865+3_865+13del MANE Select	NP_000119.1:n.865+3_865+13del