Canonical Allele Identifier: CA1519936232

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280821_186280825delinsCATTT , CM000666.2:g.186280821_186280825delinsCATTT	GRCh38
NC_000004.11:g.187201975_187201979delinsCATTT , CM000666.1:g.187201975_187201979delinsCATTT	GRCh37
NC_000004.10:g.187438969_187438973delinsCATTT	NCBI36
NG_008051.1:g.19858_19862delinsCATTT , LRG_583:g.19858_19862delinsCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1135+241_1135+245delinsCATTT MANE Select	ENSP00000384957.2:n.1135+241_1135+245delinsCATTT
ENST00000264692.8:c.973+241_973+245delinsCATTT	ENSP00000264692.5:n.973+241_973+245delinsCATTT
ENST00000403665.6:c.1135+241_1135+245delinsCATTT	ENSP00000384957.2:n.1135+241_1135+245delinsCATTT
ENST00000452239.1:c.582+241_582+245delinsCATTT
NM_000128.3:c.1135+241_1135+245delinsCATTT , LRG_583t1:c.1135+241_1135+245delinsCATTT	NP_000119.1:n.1135+241_1135+245delinsCATTT
XM_005262821.2:c.1138+241_1138+245delinsCATTT	XP_005262878.1:n.1138+241_1138+245delinsCATTT
XM_005262822.2:c.1138+241_1138+245delinsCATTT	XP_005262879.1:n.1138+241_1138+245delinsCATTT
XM_005262823.2:c.868+241_868+245delinsCATTT	XP_005262880.1:n.868+241_868+245delinsCATTT
XM_005262824.1:c.1138+241_1138+245delinsCATTT	XP_005262881.1:n.1138+241_1138+245delinsCATTT
XM_006714137.1:c.1090+241_1090+245delinsCATTT	XP_006714200.1:n.1090+241_1090+245delinsCATTT
XR_938706.1:n.1490+241_1490+245delinsCATTT
XR_938707.1:n.1490+241_1490+245delinsCATTT
XM_005262821.4:c.1138+241_1138+245delinsCATTT	XP_005262878.1:n.1138+241_1138+245delinsCATTT
XM_005262822.4:c.1138+241_1138+245delinsCATTT	XP_005262879.1:n.1138+241_1138+245delinsCATTT
XM_005262823.4:c.868+241_868+245delinsCATTT	XP_005262880.1:n.868+241_868+245delinsCATTT
XM_006714137.3:c.1090+241_1090+245delinsCATTT	XP_006714200.1:n.1090+241_1090+245delinsCATTT
XM_017007884.2:c.1138+241_1138+245delinsCATTT	XP_016863373.1:n.1138+241_1138+245delinsCATTT
XM_017007885.2:c.1138+241_1138+245delinsCATTT	XP_016863374.1:n.1138+241_1138+245delinsCATTT
XM_017007886.2:c.1135+241_1135+245delinsCATTT	XP_016863375.1:n.1135+241_1135+245delinsCATTT
XR_001741172.2:n.1556+241_1556+245delinsCATTT
NM_000128.4:c.1135+241_1135+245delinsCATTT MANE Select	NP_000119.1:n.1135+241_1135+245delinsCATTT