Canonical Allele Identifier: CA2582341248

Gene: F11

Linked Data

• ClinVar Variation Id: 2581513
• ClinVar RCV Id: RCV003331918

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276387_186276415delinsT , CM000666.2:g.186276387_186276415delinsT	GRCh38
NC_000004.11:g.187197541_187197569delinsT , CM000666.1:g.187197541_187197569delinsT	GRCh37
NC_000004.10:g.187434535_187434563delinsT	NCBI36
NG_008051.1:g.15424_15452delinsT , LRG_583:g.15424_15452delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.752_755+25delinsT
ENST00000264692.8:c.590_593+25delinsT
ENST00000403665.6:c.752_755+25delinsT
ENST00000452239.1:c.199_202+25delinsT
NM_000128.3:c.752_755+25delinsT , LRG_583t1:c.752_755+25delinsT
XM_005262821.2:c.752_755+25delinsT
XM_005262822.2:c.752_755+25delinsT
XM_005262823.2:c.485+2112_485+2140delinsT	XP_005262880.1:n.485+2112_485+2140delinsT
XM_005262824.1:c.752_755+25delinsT
XM_006714137.1:c.752_755+25delinsT
XR_938706.1:n.1104_1107+25delinsT
XR_938707.1:n.1104_1107+25delinsT
XM_005262821.4:c.752_755+25delinsT
XM_005262822.4:c.752_755+25delinsT
XM_005262823.4:c.485+2112_485+2140delinsT	XP_005262880.1:n.485+2112_485+2140delinsT
XM_006714137.3:c.752_755+25delinsT
XM_017007884.2:c.752_755+25delinsT
XM_017007885.2:c.752_755+25delinsT
XM_017007886.2:c.752_755+25delinsT
XR_001741172.2:n.1085_1088+25delinsT
NM_000128.4:c.752_755+25delinsT