Canonical Allele Identifier: CA1519934146
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276221_186276233delinsCGTCGCGCAGCTT , CM000666.2:g.186276221_186276233delinsCGTCGCGCAGCTT GRCh38
NC_000004.11:g.187197375_187197387delinsCGTCGCGCAGCTT , CM000666.1:g.187197375_187197387delinsCGTCGCGCAGCTT GRCh37
NC_000004.10:g.187434369_187434381delinsCGTCGCGCAGCTT NCBI36
NG_008051.1:g.15258_15270delinsCGTCGCGCAGCTT , LRG_583:g.15258_15270delinsCGTCGCGCAGCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.596-10_598delinsCGTCGCGCAGCTT
ENST00000264692.8:c.434-10_436delinsCGTCGCGCAGCTT
ENST00000403665.6:c.596-10_598delinsCGTCGCGCAGCTT
ENST00000452239.1:c.43-10_45delinsCGTCGCGCAGCTT
NM_000128.3:c.596-10_598delinsCGTCGCGCAGCTT , LRG_583t1:c.596-10_598delinsCGTCGCGCAGCTT
XM_005262821.2:c.596-10_598delinsCGTCGCGCAGCTT
XM_005262822.2:c.596-10_598delinsCGTCGCGCAGCTT
XM_005262823.2:c.485+1946_485+1958delinsCGTCGCGCAGCTT XP_005262880.1:n.485+1946_485+1958delinsCGTCGCGCAGCTT
XM_005262824.1:c.596-10_598delinsCGTCGCGCAGCTT
XM_006714137.1:c.596-10_598delinsCGTCGCGCAGCTT
XR_938706.1:n.948-10_950delinsCGTCGCGCAGCTT
XR_938707.1:n.948-10_950delinsCGTCGCGCAGCTT
XM_005262821.4:c.596-10_598delinsCGTCGCGCAGCTT
XM_005262822.4:c.596-10_598delinsCGTCGCGCAGCTT
XM_005262823.4:c.485+1946_485+1958delinsCGTCGCGCAGCTT XP_005262880.1:n.485+1946_485+1958delinsCGTCGCGCAGCTT
XM_006714137.3:c.596-10_598delinsCGTCGCGCAGCTT
XM_017007884.2:c.596-10_598delinsCGTCGCGCAGCTT
XM_017007885.2:c.596-10_598delinsCGTCGCGCAGCTT
XM_017007886.2:c.596-10_598delinsCGTCGCGCAGCTT
XR_001741172.2:n.929-10_931delinsCGTCGCGCAGCTT
NM_000128.4:c.596-10_598delinsCGTCGCGCAGCTT