Canonical Allele Identifier: CA1519938443

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285553_186285557delinsATAAT , CM000666.2:g.186285553_186285557delinsATAAT	GRCh38
NC_000004.11:g.187206707_187206711delinsATAAT , CM000666.1:g.187206707_187206711delinsATAAT	GRCh37
NC_000004.10:g.187443701_187443705delinsATAAT	NCBI36
NG_008051.1:g.24590_24594delinsATAAT , LRG_583:g.24590_24594delinsATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1305-85_1305-81delinsATAAT MANE Select	ENSP00000384957.2:n.1305-85_1305-81delinsATAAT
ENST00000264692.8:c.1143-85_1143-81delinsATAAT	ENSP00000264692.5:n.1143-85_1143-81delinsATAAT
ENST00000403665.6:c.1305-85_1305-81delinsATAAT	ENSP00000384957.2:n.1305-85_1305-81delinsATAAT
NM_000128.3:c.1305-85_1305-81delinsATAAT , LRG_583t1:c.1305-85_1305-81delinsATAAT	NP_000119.1:n.1305-85_1305-81delinsATAAT
XM_005262821.2:c.1308-85_1308-81delinsATAAT	XP_005262878.1:n.1308-85_1308-81delinsATAAT
XM_005262822.2:c.1308-85_1308-81delinsATAAT	XP_005262879.1:n.1308-85_1308-81delinsATAAT
XM_005262823.2:c.1038-85_1038-81delinsATAAT	XP_005262880.1:n.1038-85_1038-81delinsATAAT
XM_005262824.1:c.1308-85_1308-81delinsATAAT	XP_005262881.1:n.1308-85_1308-81delinsATAAT
XM_006714137.1:c.1260-85_1260-81delinsATAAT	XP_006714200.1:n.1260-85_1260-81delinsATAAT
XR_938706.1:n.1713-85_1713-81delinsATAAT
XR_938707.1:n.1713-85_1713-81delinsATAAT
XM_005262821.4:c.1308-85_1308-81delinsATAAT	XP_005262878.1:n.1308-85_1308-81delinsATAAT
XM_005262822.4:c.1308-85_1308-81delinsATAAT	XP_005262879.1:n.1308-85_1308-81delinsATAAT
XM_005262823.4:c.1038-85_1038-81delinsATAAT	XP_005262880.1:n.1038-85_1038-81delinsATAAT
XM_006714137.3:c.1260-85_1260-81delinsATAAT	XP_006714200.1:n.1260-85_1260-81delinsATAAT
XR_001741172.2:n.1779-85_1779-81delinsATAAT
NM_000128.4:c.1305-85_1305-81delinsATAAT MANE Select	NP_000119.1:n.1305-85_1305-81delinsATAAT