Canonical Allele Identifier: CA2672902976

Gene: F11

Linked Data

• gnomAD v4: 4-186285764-C-CCATTTCTGTGTGGAAGAGGATTACAAGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285764_186285765insCATTTCTGTGTGGAAGAGGATTACAAGCA , CM000666.2:g.186285764_186285765insCATTTCTGTGTGGAAGAGGATTACAAGCA	GRCh38
NC_000004.11:g.187206918_187206919insCATTTCTGTGTGGAAGAGGATTACAAGCA , CM000666.1:g.187206918_187206919insCATTTCTGTGTGGAAGAGGATTACAAGCA	GRCh37
NC_000004.10:g.187443912_187443913insCATTTCTGTGTGGAAGAGGATTACAAGCA	NCBI36
NG_008051.1:g.24801_24802insCATTTCTGTGTGGAAGAGGATTACAAGCA , LRG_583:g.24801_24802insCATTTCTGTGTGGAAGAGGATTACAAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1431_1432insCATTTCTGTGTGGAAGAGGATTACAAGCA MANE Select	ENSP00000384957.2:p.Gly478HisfsTer17
ENST00000264691.4:c.127_128insCATTTCTGTGTGGAAGAGGATTACAAGCA
ENST00000264692.8:c.1269_1270insCATTTCTGTGTGGAAGAGGATTACAAGCA	ENSP00000264692.5:p.Gly424HisfsTer17
ENST00000403665.6:c.1431_1432insCATTTCTGTGTGGAAGAGGATTACAAGCA	ENSP00000384957.2:p.Gly478HisfsTer17
NM_000128.3:c.1431_1432insCATTTCTGTGTGGAAGAGGATTACAAGCA , LRG_583t1:c.1431_1432insCATTTCTGTGTGGAAGAGGATTACAAGCA	NP_000119.1:p.Gly478HisfsTer17
XM_005262821.2:c.1434_1435insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262878.1:p.Gly479HisfsTer17
XM_005262822.2:c.1434_1435insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262879.1:p.Gly479HisfsTer17
XM_005262823.2:c.1164_1165insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262880.1:p.Gly389HisfsTer17
XM_005262824.1:c.1434_1435insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262881.1:p.Gly479HisfsTer17
XM_006714137.1:c.1386_1387insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_006714200.1:p.Gly463HisfsTer17
XR_938706.1:n.1839_1840insCATTTCTGTGTGGAAGAGGATTACAAGCA
XR_938707.1:n.1839_1840insCATTTCTGTGTGGAAGAGGATTACAAGCA
XM_005262821.4:c.1434_1435insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262878.1:p.Gly479HisfsTer17
XM_005262822.4:c.1434_1435insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262879.1:p.Gly479HisfsTer17
XM_005262823.4:c.1164_1165insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_005262880.1:p.Gly389HisfsTer17
XM_006714137.3:c.1386_1387insCATTTCTGTGTGGAAGAGGATTACAAGCA	XP_006714200.1:p.Gly463HisfsTer17
XR_001741172.2:n.1905_1906insCATTTCTGTGTGGAAGAGGATTACAAGCA
NM_000128.4:c.1431_1432insCATTTCTGTGTGGAAGAGGATTACAAGCA MANE Select	NP_000119.1:p.Gly478HisfsTer17