Canonical Allele Identifier: CA1820845769
Gene: DNAAF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572395T= , CM000670.2:g.132572395T= GRCh38
NC_000008.10:g.133584643T= , CM000670.1:g.133584643T= GRCh37
NC_000008.9:g.133653825T= NCBI36
NG_033068.1:g.108221A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.1312A= MANE Select ENSP00000484634.1:p.Thr438=
ENST00000250173.5:c.*176A= ENSP00000250173.2:n.*176A=
ENST00000518642.5:c.*176A= ENSP00000428610.1:n.*176A=
ENST00000519595.5:c.1312A= ENSP00000429791.1:p.Thr438=
ENST00000522789.5:c.532A= ENSP00000428015.1:p.Thr178=
ENST00000618342.1:c.1312A= ENSP00000484802.1:p.Thr438=
ENST00000620350.4:c.1312A= ENSP00000484634.1:p.Thr438=
NM_012472.4:c.1312A= NP_036604.2:p.Thr438=
NR_073525.1:n.1536A=
XM_006716538.2:c.1330A= XP_006716601.2:p.Thr444=
XM_011516950.1:c.1270A= XP_011515252.1:p.Thr424=
XM_011516952.1:c.1066A= XP_011515254.1:p.Thr356=
XM_011516953.1:c.952A= XP_011515255.1:p.Thr318=
XM_011516954.1:c.952A= XP_011515256.1:p.Thr318=
XR_428377.2:n.1564A=
NM_001321961.1:c.1252A= NP_001308890.1:p.Thr418=
NM_001321962.1:c.1066A= NP_001308891.1:p.Thr356=
NM_001321963.1:c.952A= NP_001308892.1:p.Thr318=
NM_001321964.1:c.952A= NP_001308893.1:p.Thr318=
NM_001321965.1:c.952A= NP_001308894.1:p.Thr318=
NM_001321966.1:c.892A= NP_001308895.1:p.Thr298=
NM_012472.5:c.1312A= NP_036604.2:p.Thr438=
NR_073525.2:n.1536A=
NR_135905.1:n.1525A=
NR_135906.1:n.966A=
NR_135907.1:n.1212A=
NR_135908.1:n.906A=
NR_135909.1:n.1330A=
NR_135910.1:n.1637A=
NR_135911.1:n.1716A=
NR_135912.1:n.2275A=
NR_135913.1:n.1962A=
XM_006716538.3:c.1330A= XP_006716601.2:p.Thr444=
XM_011516950.2:c.1270A= XP_011515252.1:p.Thr424=
XM_017013296.1:c.1210A= XP_016868785.1:p.Thr404=
XM_017013297.1:c.952A= XP_016868786.1:p.Thr318=
XM_017013298.1:c.952A= XP_016868787.1:p.Thr318=
NM_012472.6:c.1312A= MANE Select NP_036604.2:p.Thr438=
NM_001321961.2:c.1252A= NP_001308890.1:p.Thr418=
NM_001321962.2:c.1066A= NP_001308891.1:p.Thr356=
NM_001321963.2:c.952A= NP_001308892.1:p.Thr318=
NM_001321964.2:c.952A= NP_001308893.1:p.Thr318=
NM_001321965.2:c.952A= NP_001308894.1:p.Thr318=
NM_001321966.2:c.892A= NP_001308895.1:p.Thr298=
NR_073525.3:n.1464A=
NR_135905.2:n.1453A=
NR_135906.2:n.894A=
NR_135907.2:n.1140A=
NR_135908.2:n.834A=
NR_135909.2:n.1350A=
NR_135910.2:n.1700A=
NR_135911.2:n.1820A=
NR_135912.2:n.2379A=
NR_135913.2:n.2066A=