Canonical Allele Identifier: CA1519938460
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285592_186285593delinsAT , CM000666.2:g.186285592_186285593delinsAT GRCh38
NC_000004.11:g.187206746_187206747delinsAT , CM000666.1:g.187206746_187206747delinsAT GRCh37
NC_000004.10:g.187443740_187443741delinsAT NCBI36
NG_008051.1:g.24629_24630delinsAT , LRG_583:g.24629_24630delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1305-46_1305-45delinsAT MANE Select ENSP00000384957.2:n.1305-46_1305-45delinsAT
ENST00000264692.8:c.1143-46_1143-45delinsAT ENSP00000264692.5:n.1143-46_1143-45delinsAT
ENST00000403665.6:c.1305-46_1305-45delinsAT ENSP00000384957.2:n.1305-46_1305-45delinsAT
NM_000128.3:c.1305-46_1305-45delinsAT , LRG_583t1:c.1305-46_1305-45delinsAT NP_000119.1:n.1305-46_1305-45delinsAT
XM_005262821.2:c.1308-46_1308-45delinsAT XP_005262878.1:n.1308-46_1308-45delinsAT
XM_005262822.2:c.1308-46_1308-45delinsAT XP_005262879.1:n.1308-46_1308-45delinsAT
XM_005262823.2:c.1038-46_1038-45delinsAT XP_005262880.1:n.1038-46_1038-45delinsAT
XM_005262824.1:c.1308-46_1308-45delinsAT XP_005262881.1:n.1308-46_1308-45delinsAT
XM_006714137.1:c.1260-46_1260-45delinsAT XP_006714200.1:n.1260-46_1260-45delinsAT
XR_938706.1:n.1713-46_1713-45delinsAT
XR_938707.1:n.1713-46_1713-45delinsAT
XM_005262821.4:c.1308-46_1308-45delinsAT XP_005262878.1:n.1308-46_1308-45delinsAT
XM_005262822.4:c.1308-46_1308-45delinsAT XP_005262879.1:n.1308-46_1308-45delinsAT
XM_005262823.4:c.1038-46_1038-45delinsAT XP_005262880.1:n.1038-46_1038-45delinsAT
XM_006714137.3:c.1260-46_1260-45delinsAT XP_006714200.1:n.1260-46_1260-45delinsAT
XR_001741172.2:n.1779-46_1779-45delinsAT
NM_000128.4:c.1305-46_1305-45delinsAT MANE Select NP_000119.1:n.1305-46_1305-45delinsAT