Canonical Allele Identifier: CA2764876469

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280365_186280366insACACACCCAAC , CM000666.2:g.186280365_186280366insACACACCCAAC	GRCh38
NC_000004.11:g.187201519_187201520insACACACCCAAC , CM000666.1:g.187201519_187201520insACACACCCAAC	GRCh37
NC_000004.10:g.187438513_187438514insACACACCCAAC	NCBI36
NG_008051.1:g.19402_19403insACACACCCAAC , LRG_583:g.19402_19403insACACACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1008_1009insACACACCCAAC MANE Select	ENSP00000384957.2:p.Ala337ThrfsTer16
ENST00000264692.8:c.846_847insACACACCCAAC	ENSP00000264692.5:p.Ala283ThrfsTer16
ENST00000403665.6:c.1008_1009insACACACCCAAC	ENSP00000384957.2:p.Ala337ThrfsTer16
ENST00000452239.1:c.455_456insACACACCCAAC
NM_000128.3:c.1008_1009insACACACCCAAC , LRG_583t1:c.1008_1009insACACACCCAAC	NP_000119.1:p.Ala337ThrfsTer16
XM_005262821.2:c.1008_1009insACACACCCAAC	XP_005262878.1:p.Ala337ThrfsTer17
XM_005262822.2:c.1008_1009insACACACCCAAC	XP_005262879.1:p.Ala337ThrfsTer17
XM_005262823.2:c.738_739insACACACCCAAC	XP_005262880.1:p.Ala247ThrfsTer17
XM_005262824.1:c.1008_1009insACACACCCAAC	XP_005262881.1:p.Ala337ThrfsTer17
XM_006714137.1:c.960_961insACACACCCAAC	XP_006714200.1:p.Ala321ThrfsTer17
XR_938706.1:n.1360_1361insACACACCCAAC
XR_938707.1:n.1360_1361insACACACCCAAC
XM_005262821.4:c.1008_1009insACACACCCAAC	XP_005262878.1:p.Ala337ThrfsTer17
XM_005262822.4:c.1008_1009insACACACCCAAC	XP_005262879.1:p.Ala337ThrfsTer17
XM_005262823.4:c.738_739insACACACCCAAC	XP_005262880.1:p.Ala247ThrfsTer17
XM_006714137.3:c.960_961insACACACCCAAC	XP_006714200.1:p.Ala321ThrfsTer17
XM_017007884.2:c.1008_1009insACACACCCAAC	XP_016863373.1:p.Ala337ThrfsTer17
XM_017007885.2:c.1008_1009insACACACCCAAC	XP_016863374.1:p.Ala337ThrfsTer17
XM_017007886.2:c.1008_1009insACACACCCAAC	XP_016863375.1:p.Ala337ThrfsTer16
XR_001741172.2:n.1341_1342insACACACCCAAC
NM_000128.4:c.1008_1009insACACACCCAAC MANE Select	NP_000119.1:p.Ala337ThrfsTer16