Canonical Allele Identifier: CA645540589

Gene: F11

Linked Data

• COSMIC: COSM402547

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276390_186276391delinsTT , CM000666.2:g.186276390_186276391delinsTT	GRCh38
NC_000004.11:g.187197544_187197545delinsTT , CM000666.1:g.187197544_187197545delinsTT	GRCh37
NC_000004.10:g.187434538_187434539delinsTT	NCBI36
NG_008051.1:g.15427_15428delinsTT , LRG_583:g.15427_15428delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.755_755+1delinsTT
ENST00000264692.8:c.593_593+1delinsTT
ENST00000403665.6:c.755_755+1delinsTT
ENST00000452239.1:c.202_202+1delinsTT
NM_000128.3:c.755_755+1delinsTT , LRG_583t1:c.755_755+1delinsTT
XM_005262821.2:c.755_755+1delinsTT
XM_005262822.2:c.755_755+1delinsTT
XM_005262823.2:c.485+2115_485+2116delinsTT	XP_005262880.1:n.485+2115_485+2116delinsTT
XM_005262824.1:c.755_755+1delinsTT
XM_006714137.1:c.755_755+1delinsTT
XR_938706.1:n.1107_1107+1delinsTT
XR_938707.1:n.1107_1107+1delinsTT
XM_005262821.4:c.755_755+1delinsTT
XM_005262822.4:c.755_755+1delinsTT
XM_005262823.4:c.485+2115_485+2116delinsTT	XP_005262880.1:n.485+2115_485+2116delinsTT
XM_006714137.3:c.755_755+1delinsTT
XM_017007884.2:c.755_755+1delinsTT
XM_017007885.2:c.755_755+1delinsTT
XM_017007886.2:c.755_755+1delinsTT
XR_001741172.2:n.1088_1088+1delinsTT
NM_000128.4:c.755_755+1delinsTT