Canonical Allele Identifier: CA2201723745
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520727_1520742delinsCCTTGGCCACGGTCAT , CM000678.2:g.1520727_1520742delinsCCTTGGCCACGGTCAT GRCh38
NC_000016.9:g.1570728_1570743delinsCCTTGGCCACGGTCAT , CM000678.1:g.1570728_1570743delinsCCTTGGCCACGGTCAT GRCh37
NC_000016.8:g.1510729_1510744delinsCCTTGGCCACGGTCAT NCBI36
NG_032783.1:g.96367_96382delinsATGACCGTGGCCAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.3520_3535delinsATGACCGTGGCCAAGG MANE Select ENSP00000406012.2:p.Met1174=
ENST00000361339.9:c.1102_1117delinsATGACCGTGGCCAAGG ENSP00000354895.5:p.Met368=
ENST00000397417.6:c.*1958_*1973delinsATGACCGTGGCCAAGG ENSP00000380562.2:n.*1958_*1973delinsATGA...
ENST00000426508.6:c.3520_3535delinsATGACCGTGGCCAAGG ENSP00000406012.2:p.Met1174=
ENST00000565298.5:n.3344_3359delinsATGACCGTGGCCAAGG
NM_014714.3:c.3520_3535delinsATGACCGTGGCCAAGG NP_055529.2:p.Met1174=
XM_006720989.2:c.3520_3535delinsATGACCGTGGCCAAGG XP_006721052.1:p.Met1174=
XM_006720990.2:c.3520_3535delinsATGACCGTGGCCAAGG XP_006721053.1:p.Met1174=
XM_006720991.2:c.3520_3535delinsATGACCGTGGCCAAGG XP_006721054.1:p.Met1174=
XM_006720992.2:c.1153_1168delinsATGACCGTGGCCAAGG XP_006721055.1:p.Met385=
XM_011522766.1:c.3274_3289delinsATGACCGTGGCCAAGG XP_011521068.1:p.Met1092=
XM_011522767.1:c.2545_2560delinsATGACCGTGGCCAAGG XP_011521069.1:p.Met849=
XM_006720990.3:c.3520_3535delinsATGACCGTGGCCAAGG XP_006721053.1:p.Met1174=
XM_006720991.3:c.3520_3535delinsATGACCGTGGCCAAGG XP_006721054.1:p.Met1174=
XM_006720992.3:c.1153_1168delinsATGACCGTGGCCAAGG XP_006721055.1:p.Met385=
XM_011522766.3:c.3274_3289delinsATGACCGTGGCCAAGG XP_011521068.1:p.Met1092=
XM_011522767.2:c.2545_2560delinsATGACCGTGGCCAAGG XP_011521069.1:p.Met849=
XM_017023910.1:c.3520_3535delinsATGACCGTGGCCAAGG XP_016879399.1:p.Met1174=
XM_017023911.1:c.1705_1720delinsATGACCGTGGCCAAGG XP_016879400.1:p.Met569=
NM_014714.4:c.3520_3535delinsATGACCGTGGCCAAGG MANE Select NP_055529.2:p.Met1174=