Canonical Allele Identifier: CA1820845726
Gene: DNAAF11 HGNC NCBI

Linked Data

dbSNP Id: rs144068846

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572301A>G , CM000670.2:g.132572301A>G GRCh38
NC_000008.10:g.133584549A>G , CM000670.1:g.133584549A>G GRCh37
NC_000008.9:g.133653731A>G NCBI36
NG_033068.1:g.108315T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.*5T>C MANE Select ENSP00000484634.1:n.*5T>C
ENST00000250173.5:c.*270T>C ENSP00000250173.2:n.*270T>C
ENST00000518642.5:c.*270T>C ENSP00000428610.1:n.*270T>C
ENST00000519595.5:c.*5T>C ENSP00000429791.1:n.*5T>C
ENST00000522789.5:c.626T>C ENSP00000428015.1:n.626T>C
ENST00000618342.1:c.1406T>C ENSP00000484802.1:n.1406T>C
ENST00000620350.4:c.*5T>C ENSP00000484634.1:n.*5T>C
NM_012472.4:c.*5T>C NP_036604.2:n.*5T>C
NR_073525.1:n.1630T>C
XM_006716538.2:c.*5T>C XP_006716601.2:n.*5T>C
XM_011516950.1:c.*5T>C XP_011515252.1:n.*5T>C
XM_011516952.1:c.*5T>C XP_011515254.1:n.*5T>C
XM_011516953.1:c.*5T>C XP_011515255.1:n.*5T>C
XM_011516954.1:c.*5T>C XP_011515256.1:n.*5T>C
XR_428377.2:n.1658T>C
NM_001321961.1:c.*5T>C NP_001308890.1:n.*5T>C
NM_001321962.1:c.*5T>C NP_001308891.1:n.*5T>C
NM_001321963.1:c.*5T>C NP_001308892.1:n.*5T>C
NM_001321964.1:c.*5T>C NP_001308893.1:n.*5T>C
NM_001321965.1:c.*5T>C NP_001308894.1:n.*5T>C
NM_001321966.1:c.*5T>C NP_001308895.1:n.*5T>C
NM_012472.5:c.*5T>C NP_036604.2:n.*5T>C
NR_073525.2:n.1630T>C
NR_135905.1:n.1619T>C
NR_135906.1:n.1060T>C
NR_135907.1:n.1306T>C
NR_135908.1:n.1000T>C
NR_135909.1:n.1424T>C
NR_135910.1:n.1731T>C
NR_135911.1:n.1810T>C
NR_135912.1:n.2369T>C
NR_135913.1:n.2056T>C
XM_006716538.3:c.*5T>C XP_006716601.2:n.*5T>C
XM_011516950.2:c.*5T>C XP_011515252.1:n.*5T>C
XM_017013296.1:c.*5T>C XP_016868785.1:n.*5T>C
XM_017013297.1:c.*5T>C XP_016868786.1:n.*5T>C
XM_017013298.1:c.*5T>C XP_016868787.1:n.*5T>C
NM_012472.6:c.*5T>C MANE Select NP_036604.2:n.*5T>C
NM_001321961.2:c.*5T>C NP_001308890.1:n.*5T>C
NM_001321962.2:c.*5T>C NP_001308891.1:n.*5T>C
NM_001321963.2:c.*5T>C NP_001308892.1:n.*5T>C
NM_001321964.2:c.*5T>C NP_001308893.1:n.*5T>C
NM_001321965.2:c.*5T>C NP_001308894.1:n.*5T>C
NM_001321966.2:c.*5T>C NP_001308895.1:n.*5T>C
NR_073525.3:n.1558T>C
NR_135905.2:n.1547T>C
NR_135906.2:n.988T>C
NR_135907.2:n.1234T>C
NR_135908.2:n.928T>C
NR_135909.2:n.1444T>C
NR_135910.2:n.1794T>C
NR_135911.2:n.1914T>C
NR_135912.2:n.2473T>C
NR_135913.2:n.2160T>C