Canonical Allele Identifier: CA1519936227
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280808_186280813delinsCTTTAA , CM000666.2:g.186280808_186280813delinsCTTTAA GRCh38
NC_000004.11:g.187201962_187201967delinsCTTTAA , CM000666.1:g.187201962_187201967delinsCTTTAA GRCh37
NC_000004.10:g.187438956_187438961delinsCTTTAA NCBI36
NG_008051.1:g.19845_19850delinsCTTTAA , LRG_583:g.19845_19850delinsCTTTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1135+228_1135+233delinsCTTTAA MANE Select ENSP00000384957.2:n.1135+228_1135+233delinsCTTTAA
ENST00000264692.8:c.973+228_973+233delinsCTTTAA ENSP00000264692.5:n.973+228_973+233delinsCTTTAA
ENST00000403665.6:c.1135+228_1135+233delinsCTTTAA ENSP00000384957.2:n.1135+228_1135+233delinsCTTTAA
ENST00000452239.1:c.582+228_582+233delinsCTTTAA
NM_000128.3:c.1135+228_1135+233delinsCTTTAA , LRG_583t1:c.1135+228_1135+233delinsCTTTAA NP_000119.1:n.1135+228_1135+233delinsCTTTAA
XM_005262821.2:c.1138+228_1138+233delinsCTTTAA XP_005262878.1:n.1138+228_1138+233delinsCTTTAA
XM_005262822.2:c.1138+228_1138+233delinsCTTTAA XP_005262879.1:n.1138+228_1138+233delinsCTTTAA
XM_005262823.2:c.868+228_868+233delinsCTTTAA XP_005262880.1:n.868+228_868+233delinsCTTTAA
XM_005262824.1:c.1138+228_1138+233delinsCTTTAA XP_005262881.1:n.1138+228_1138+233delinsCTTTAA
XM_006714137.1:c.1090+228_1090+233delinsCTTTAA XP_006714200.1:n.1090+228_1090+233delinsCTTTAA
XR_938706.1:n.1490+228_1490+233delinsCTTTAA
XR_938707.1:n.1490+228_1490+233delinsCTTTAA
XM_005262821.4:c.1138+228_1138+233delinsCTTTAA XP_005262878.1:n.1138+228_1138+233delinsCTTTAA
XM_005262822.4:c.1138+228_1138+233delinsCTTTAA XP_005262879.1:n.1138+228_1138+233delinsCTTTAA
XM_005262823.4:c.868+228_868+233delinsCTTTAA XP_005262880.1:n.868+228_868+233delinsCTTTAA
XM_006714137.3:c.1090+228_1090+233delinsCTTTAA XP_006714200.1:n.1090+228_1090+233delinsCTTTAA
XM_017007884.2:c.1138+228_1138+233delinsCTTTAA XP_016863373.1:n.1138+228_1138+233delinsCTTTAA
XM_017007885.2:c.1138+228_1138+233delinsCTTTAA XP_016863374.1:n.1138+228_1138+233delinsCTTTAA
XM_017007886.2:c.1135+228_1135+233delinsCTTTAA XP_016863375.1:n.1135+228_1135+233delinsCTTTAA
XR_001741172.2:n.1556+228_1556+233delinsCTTTAA
NM_000128.4:c.1135+228_1135+233delinsCTTTAA MANE Select NP_000119.1:n.1135+228_1135+233delinsCTTTAA