Canonical Allele Identifier: CA2396130866
Gene: ARVCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19972891_19972910delinsGCAGGGAATGGAAGGAAGGC , CM000684.2:g.19972891_19972910delinsGCAGGGAATGGAAGGAAGGC GRCh38
NC_000022.10:g.19960414_19960433delinsGCAGGGAATGGAAGGAAGGC , CM000684.1:g.19960414_19960433delinsGCAGGGAATGGAAGGAAGGC GRCh37
NC_000022.9:g.18340414_18340433delinsGCAGGGAATGGAAGGAAGGC NCBI36
NG_023326.1:g.48877_48896delinsGCCTTCCTTCCATTCCCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC MANE Select ENSP00000263207.3:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC...
ENST00000263207.7:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC ENSP00000263207.3:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC...
ENST00000401994.5:c.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC ENSP00000384341.1:n.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC...
ENST00000406259.1:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC ENSP00000385444.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC...
ENST00000406522.5:c.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC ENSP00000384732.1:n.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC...
ENST00000495096.5:n.1472+15_1472+34delinsGCCTTCCTTCCATTCCCTGC
NM_001670.2:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC NP_001661.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261242.1:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261299.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261243.3:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261300.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261244.3:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261301.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724243.1:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC XP_006724306.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724245.2:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC XP_006724308.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724246.2:c.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC XP_006724309.1:n.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724247.2:c.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC XP_006724310.1:n.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724248.2:c.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC XP_006724311.1:n.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530179.1:c.2517+15_2517+34delinsGCCTTCCTTCCATTCCCTGC XP_011528481.1:n.2517+15_2517+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530180.1:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC XP_011528482.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530182.1:c.1116+15_1116+34delinsGCCTTCCTTCCATTCCCTGC XP_011528484.1:n.1116+15_1116+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530183.1:c.1098+15_1098+34delinsGCCTTCCTTCCATTCCCTGC XP_011528485.1:n.1098+15_1098+34delinsGCCTTCCTTCCATTCCCTGC
XR_937863.1:n.2637+15_2637+34delinsGCCTTCCTTCCATTCCCTGC
XR_937864.1:n.2637+15_2637+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261242.3:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261299.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261243.4:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261300.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_005261244.4:c.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC XP_005261301.1:n.2532+15_2532+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724243.3:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC XP_006724306.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724245.3:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC XP_006724308.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724246.4:c.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC XP_006724309.1:n.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724247.4:c.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC XP_006724310.1:n.2361+15_2361+34delinsGCCTTCCTTCCATTCCCTGC
XM_006724248.4:c.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC XP_006724311.1:n.2343+15_2343+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530179.3:c.2517+15_2517+34delinsGCCTTCCTTCCATTCCCTGC XP_011528481.1:n.2517+15_2517+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530182.3:c.1116+15_1116+34delinsGCCTTCCTTCCATTCCCTGC XP_011528484.1:n.1116+15_1116+34delinsGCCTTCCTTCCATTCCCTGC
XM_011530183.3:c.1098+15_1098+34delinsGCCTTCCTTCCATTCCCTGC XP_011528485.1:n.1098+15_1098+34delinsGCCTTCCTTCCATTCCCTGC
XM_024452249.1:c.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC XP_024308017.1:n.2304+15_2304+34delinsGCCTTCCTTCCATTCCCTGC
XR_937863.2:n.2637+15_2637+34delinsGCCTTCCTTCCATTCCCTGC
NM_001670.3:c.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC MANE Select NP_001661.1:n.2550+15_2550+34delinsGCCTTCCTTCCATTCCCTGC