Canonical Allele Identifier: CA2526275265
Gene: DNAAF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572347_132572348insT , CM000670.2:g.132572347_132572348insT GRCh38
NC_000008.10:g.133584595_133584596insT , CM000670.1:g.133584595_133584596insT GRCh37
NC_000008.9:g.133653777_133653778insT NCBI36
NG_033068.1:g.108268_108269insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.1359_1360insA MANE Select ENSP00000484634.1:p.Pro454ThrfsTer4
ENST00000250173.5:c.*223_*224insA ENSP00000250173.2:n.*223_*224insA
ENST00000518642.5:c.*223_*224insA ENSP00000428610.1:n.*223_*224insA
ENST00000519595.5:c.1359_1360insA ENSP00000429791.1:p.Pro454ThrfsTer4
ENST00000522789.5:c.579_580insA ENSP00000428015.1:p.Pro194ThrfsTer4
ENST00000618342.1:c.1359_1360insA ENSP00000484802.1:p.Pro454ThrfsTer4
ENST00000620350.4:c.1359_1360insA ENSP00000484634.1:p.Pro454ThrfsTer4
NM_012472.4:c.1359_1360insA NP_036604.2:p.Pro454ThrfsTer4
NR_073525.1:n.1583_1584insA
XM_006716538.2:c.1377_1378insA XP_006716601.2:p.Pro460ThrfsTer4
XM_011516950.1:c.1317_1318insA XP_011515252.1:p.Pro440ThrfsTer4
XM_011516952.1:c.1113_1114insA XP_011515254.1:p.Pro372ThrfsTer4
XM_011516953.1:c.999_1000insA XP_011515255.1:p.Pro334ThrfsTer4
XM_011516954.1:c.999_1000insA XP_011515256.1:p.Pro334ThrfsTer4
XR_428377.2:n.1611_1612insA
NM_001321961.1:c.1299_1300insA NP_001308890.1:p.Pro434ThrfsTer4
NM_001321962.1:c.1113_1114insA NP_001308891.1:p.Pro372ThrfsTer4
NM_001321963.1:c.999_1000insA NP_001308892.1:p.Pro334ThrfsTer4
NM_001321964.1:c.999_1000insA NP_001308893.1:p.Pro334ThrfsTer4
NM_001321965.1:c.999_1000insA NP_001308894.1:p.Pro334ThrfsTer4
NM_001321966.1:c.939_940insA NP_001308895.1:p.Pro314ThrfsTer4
NM_012472.5:c.1359_1360insA NP_036604.2:p.Pro454ThrfsTer4
NR_073525.2:n.1583_1584insA
NR_135905.1:n.1572_1573insA
NR_135906.1:n.1013_1014insA
NR_135907.1:n.1259_1260insA
NR_135908.1:n.953_954insA
NR_135909.1:n.1377_1378insA
NR_135910.1:n.1684_1685insA
NR_135911.1:n.1763_1764insA
NR_135912.1:n.2322_2323insA
NR_135913.1:n.2009_2010insA
XM_006716538.3:c.1377_1378insA XP_006716601.2:p.Pro460ThrfsTer4
XM_011516950.2:c.1317_1318insA XP_011515252.1:p.Pro440ThrfsTer4
XM_017013296.1:c.1257_1258insA XP_016868785.1:p.Pro420ThrfsTer4
XM_017013297.1:c.999_1000insA XP_016868786.1:p.Pro334ThrfsTer4
XM_017013298.1:c.999_1000insA XP_016868787.1:p.Pro334ThrfsTer4
NM_012472.6:c.1359_1360insA MANE Select NP_036604.2:p.Pro454ThrfsTer4
NM_001321961.2:c.1299_1300insA NP_001308890.1:p.Pro434ThrfsTer4
NM_001321962.2:c.1113_1114insA NP_001308891.1:p.Pro372ThrfsTer4
NM_001321963.2:c.999_1000insA NP_001308892.1:p.Pro334ThrfsTer4
NM_001321964.2:c.999_1000insA NP_001308893.1:p.Pro334ThrfsTer4
NM_001321965.2:c.999_1000insA NP_001308894.1:p.Pro334ThrfsTer4
NM_001321966.2:c.939_940insA NP_001308895.1:p.Pro314ThrfsTer4
NR_073525.3:n.1511_1512insA
NR_135905.2:n.1500_1501insA
NR_135906.2:n.941_942insA
NR_135907.2:n.1187_1188insA
NR_135908.2:n.881_882insA
NR_135909.2:n.1397_1398insA
NR_135910.2:n.1747_1748insA
NR_135911.2:n.1867_1868insA
NR_135912.2:n.2426_2427insA
NR_135913.2:n.2113_2114insA