Canonical Allele Identifier: CA2573957500
Gene: NPHS2 HGNC NCBI
AXDND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179551316_179551317del , CM000663.2:g.179551316_179551317del GRCh38
NC_000001.10:g.179520451_179520452del , CM000663.1:g.179520451_179520452del GRCh37
NC_000001.9:g.177787074_177787075del NCBI36
NG_007535.1:g.29634_29635del , LRG_887:g.29634_29635del
NG_033075.1:g.190597_190598del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367615.9:c.1009_1010del (NPHS2) MANE Select ENSP00000356587.4:p.Thr337CysfsTer8
ENST00000367618.8:c.3032-3196_3032-3195del (AXDND1) MANE Select ENSP00000356590.3:n.3032-3196_3032-3195del
ENST00000367615.8:c.1009_1010del (NPHS2) ENSP00000356587.4:p.Thr337CysfsTer8
ENST00000367616.4:c.805_806del (NPHS2) ENSP00000356588.4:p.Thr269CysfsTer8
ENST00000367618.7:c.3032-3196_3032-3195del (AXDND1) ENSP00000356590.3:n.3032-3196_3032-3195del
ENST00000434088.1:c.2612-3196_2612-3195del (AXDND1) ENSP00000391716.1:n.2612-3196_2612-3195del
ENST00000457238.6:c.*1011-3196_*1011-3195del (AXDND1) ENSP00000416712.3:n.*1011-3196_*1011-3195del
ENST00000484455.1:n.471-3196_471-3195del (AXDND1)
ENST00000484883.1:n.911-3196_911-3195del (AXDND1)
ENST00000489080.1:n.250_251del (AXDND1)
ENST00000511157.5:c.*1301-3196_*1301-3195del (AXDND1) ENSP00000424373.1:n.*1301-3196_*1301-3195del
ENST00000617277.4:c.*1207-3196_*1207-3195del (AXDND1) ENSP00000482167.1:n.*1207-3196_*1207-3195del
NM_001297575.1:c.805_806del (NPHS2) NP_001284504.1:p.Thr269CysfsTer8
NM_014625.3:c.1009_1010del , LRG_887t1:c.1009_1010del (NPHS2) NP_055440.1:p.Thr337CysfsTer8
NM_144696.5:c.3032-3196_3032-3195del (AXDND1) NP_653297.3:n.3032-3196_3032-3195del
NR_073544.1:n.3152-3196_3152-3195del (AXDND1)
XM_005245483.2:c.832_833del (NPHS2) XP_005245540.1:p.Thr278CysfsTer8
XM_011509165.1:c.3038-3196_3038-3195del (AXDND1) XP_011507467.1:n.3038-3196_3038-3195del
XM_011509166.1:c.3038-3196_3038-3195del (AXDND1) XP_011507468.1:n.3038-3196_3038-3195del
XM_011509167.1:c.3038-3196_3038-3195del (AXDND1) XP_011507469.1:n.3038-3196_3038-3195del
XM_011509168.1:c.3038-3196_3038-3195del (AXDND1) XP_011507470.1:n.3038-3196_3038-3195del
XM_011509169.1:c.2975-3196_2975-3195del (AXDND1) XP_011507471.1:n.2975-3196_2975-3195del
XM_011509170.1:c.2930-3196_2930-3195del (AXDND1) XP_011507472.1:n.2930-3196_2930-3195del
XM_011509171.1:c.2912-3196_2912-3195del (AXDND1) XP_011507473.1:n.2912-3196_2912-3195del
XM_011509172.1:c.2912-3196_2912-3195del (AXDND1) XP_011507474.1:n.2912-3196_2912-3195del
XM_011509173.1:c.2912-3196_2912-3195del (AXDND1) XP_011507475.1:n.2912-3196_2912-3195del
XM_011509174.1:c.2816-3196_2816-3195del (AXDND1) XP_011507476.1:n.2816-3196_2816-3195del
XM_011509175.1:c.2810-3196_2810-3195del (AXDND1) XP_011507477.1:n.2810-3196_2810-3195del
XM_011509176.1:c.2741-3196_2741-3195del (AXDND1) XP_011507478.1:n.2741-3196_2741-3195del
XM_011509179.1:c.2402-3196_2402-3195del (AXDND1) XP_011507481.1:n.2402-3196_2402-3195del
XM_011509181.1:c.1961-3196_1961-3195del (AXDND1) XP_011507483.1:n.1961-3196_1961-3195del
XM_005245483.3:c.832_833del (NPHS2) XP_005245540.1:p.Thr278CysfsTer8
XM_011509166.3:c.3038-3196_3038-3195del (AXDND1) XP_011507468.1:n.3038-3196_3038-3195del
XM_011509167.3:c.3038-3196_3038-3195del (AXDND1) XP_011507469.1:n.3038-3196_3038-3195del
XM_011509179.2:c.2402-3196_2402-3195del (AXDND1) XP_011507481.1:n.2402-3196_2402-3195del
XM_011509181.2:c.1961-3196_1961-3195del (AXDND1) XP_011507483.1:n.1961-3196_1961-3195del
XM_017000257.2:c.2297-3196_2297-3195del (AXDND1) XP_016855746.1:n.2297-3196_2297-3195del
XM_017000258.2:c.2159-3196_2159-3195del (AXDND1) XP_016855747.1:n.2159-3196_2159-3195del
XM_017002298.1:c.676_677del (NPHS2) XP_016857787.1:p.Thr226CysfsTer8
XM_024453104.1:c.2912-3196_2912-3195del (AXDND1) XP_024308872.1:n.2912-3196_2912-3195del
XM_024453107.1:c.2912-3196_2912-3195del (AXDND1) XP_024308875.1:n.2912-3196_2912-3195del
NM_144696.6:c.3032-3196_3032-3195del (AXDND1) MANE Select NP_653297.3:n.3032-3196_3032-3195del
NM_001297575.2:c.805_806del (NPHS2) NP_001284504.1:p.Thr269CysfsTer8
NM_014625.4:c.1009_1010del (NPHS2) MANE Select NP_055440.1:p.Thr337CysfsTer8
NR_073544.2:n.3080-3196_3080-3195del (AXDND1)