Canonical Allele Identifier: CA2688630997
Gene: DNAAF11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572296G>A , CM000670.2:g.132572296G>A GRCh38
NC_000008.10:g.133584544G>A , CM000670.1:g.133584544G>A GRCh37
NC_000008.9:g.133653726G>A NCBI36
NG_033068.1:g.108320C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.*10C>T MANE Select ENSP00000484634.1:n.*10C>T
ENST00000250173.5:c.*275C>T ENSP00000250173.2:n.*275C>T
ENST00000518642.5:c.*275C>T ENSP00000428610.1:n.*275C>T
ENST00000519595.5:c.*10C>T ENSP00000429791.1:n.*10C>T
ENST00000522789.5:c.631C>T ENSP00000428015.1:n.631C>T
ENST00000618342.1:c.1411C>T ENSP00000484802.1:n.1411C>T
ENST00000620350.4:c.*10C>T ENSP00000484634.1:n.*10C>T
NM_012472.4:c.*10C>T NP_036604.2:n.*10C>T
NR_073525.1:n.1635C>T
XM_006716538.2:c.*10C>T XP_006716601.2:n.*10C>T
XM_011516950.1:c.*10C>T XP_011515252.1:n.*10C>T
XM_011516952.1:c.*10C>T XP_011515254.1:n.*10C>T
XM_011516953.1:c.*10C>T XP_011515255.1:n.*10C>T
XM_011516954.1:c.*10C>T XP_011515256.1:n.*10C>T
XR_428377.2:n.1663C>T
NM_001321961.1:c.*10C>T NP_001308890.1:n.*10C>T
NM_001321962.1:c.*10C>T NP_001308891.1:n.*10C>T
NM_001321963.1:c.*10C>T NP_001308892.1:n.*10C>T
NM_001321964.1:c.*10C>T NP_001308893.1:n.*10C>T
NM_001321965.1:c.*10C>T NP_001308894.1:n.*10C>T
NM_001321966.1:c.*10C>T NP_001308895.1:n.*10C>T
NM_012472.5:c.*10C>T NP_036604.2:n.*10C>T
NR_073525.2:n.1635C>T
NR_135905.1:n.1624C>T
NR_135906.1:n.1065C>T
NR_135907.1:n.1311C>T
NR_135908.1:n.1005C>T
NR_135909.1:n.1429C>T
NR_135910.1:n.1736C>T
NR_135911.1:n.1815C>T
NR_135912.1:n.2374C>T
NR_135913.1:n.2061C>T
XM_006716538.3:c.*10C>T XP_006716601.2:n.*10C>T
XM_011516950.2:c.*10C>T XP_011515252.1:n.*10C>T
XM_017013296.1:c.*10C>T XP_016868785.1:n.*10C>T
XM_017013297.1:c.*10C>T XP_016868786.1:n.*10C>T
XM_017013298.1:c.*10C>T XP_016868787.1:n.*10C>T
NM_012472.6:c.*10C>T MANE Select NP_036604.2:n.*10C>T
NM_001321961.2:c.*10C>T NP_001308890.1:n.*10C>T
NM_001321962.2:c.*10C>T NP_001308891.1:n.*10C>T
NM_001321963.2:c.*10C>T NP_001308892.1:n.*10C>T
NM_001321964.2:c.*10C>T NP_001308893.1:n.*10C>T
NM_001321965.2:c.*10C>T NP_001308894.1:n.*10C>T
NM_001321966.2:c.*10C>T NP_001308895.1:n.*10C>T
NR_073525.3:n.1563C>T
NR_135905.2:n.1552C>T
NR_135906.2:n.993C>T
NR_135907.2:n.1239C>T
NR_135908.2:n.933C>T
NR_135909.2:n.1449C>T
NR_135910.2:n.1799C>T
NR_135911.2:n.1919C>T
NR_135912.2:n.2478C>T
NR_135913.2:n.2165C>T