Canonical Allele Identifier: CA463074106
Gene: DNAAF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.133584641T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572393T>C , CM000670.2:g.132572393T>C GRCh38
NC_000008.10:g.133584641T>C , CM000670.1:g.133584641T>C GRCh37
NC_000008.9:g.133653823T>C NCBI36
NG_033068.1:g.108223A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.1314A>G MANE Select ENSP00000484634.1:p.Thr438=
ENST00000250173.5:c.*178A>G ENSP00000250173.2:n.*178A>G
ENST00000518642.5:c.*178A>G ENSP00000428610.1:n.*178A>G
ENST00000519595.5:c.1314A>G ENSP00000429791.1:p.Thr438=
ENST00000522789.5:c.534A>G ENSP00000428015.1:p.Thr178=
ENST00000618342.1:c.1314A>G ENSP00000484802.1:p.Thr438=
ENST00000620350.4:c.1314A>G ENSP00000484634.1:p.Thr438=
NM_012472.4:c.1314A>G NP_036604.2:p.Thr438=
NR_073525.1:n.1538A>G
XM_006716538.2:c.1332A>G XP_006716601.2:p.Thr444=
XM_011516950.1:c.1272A>G XP_011515252.1:p.Thr424=
XM_011516952.1:c.1068A>G XP_011515254.1:p.Thr356=
XM_011516953.1:c.954A>G XP_011515255.1:p.Thr318=
XM_011516954.1:c.954A>G XP_011515256.1:p.Thr318=
XR_428377.2:n.1566A>G
NM_001321961.1:c.1254A>G NP_001308890.1:p.Thr418=
NM_001321962.1:c.1068A>G NP_001308891.1:p.Thr356=
NM_001321963.1:c.954A>G NP_001308892.1:p.Thr318=
NM_001321964.1:c.954A>G NP_001308893.1:p.Thr318=
NM_001321965.1:c.954A>G NP_001308894.1:p.Thr318=
NM_001321966.1:c.894A>G NP_001308895.1:p.Thr298=
NM_012472.5:c.1314A>G NP_036604.2:p.Thr438=
NR_073525.2:n.1538A>G
NR_135905.1:n.1527A>G
NR_135906.1:n.968A>G
NR_135907.1:n.1214A>G
NR_135908.1:n.908A>G
NR_135909.1:n.1332A>G
NR_135910.1:n.1639A>G
NR_135911.1:n.1718A>G
NR_135912.1:n.2277A>G
NR_135913.1:n.1964A>G
XM_006716538.3:c.1332A>G XP_006716601.2:p.Thr444=
XM_011516950.2:c.1272A>G XP_011515252.1:p.Thr424=
XM_017013296.1:c.1212A>G XP_016868785.1:p.Thr404=
XM_017013297.1:c.954A>G XP_016868786.1:p.Thr318=
XM_017013298.1:c.954A>G XP_016868787.1:p.Thr318=
NM_012472.6:c.1314A>G MANE Select NP_036604.2:p.Thr438=
NM_001321961.2:c.1254A>G NP_001308890.1:p.Thr418=
NM_001321962.2:c.1068A>G NP_001308891.1:p.Thr356=
NM_001321963.2:c.954A>G NP_001308892.1:p.Thr318=
NM_001321964.2:c.954A>G NP_001308893.1:p.Thr318=
NM_001321965.2:c.954A>G NP_001308894.1:p.Thr318=
NM_001321966.2:c.894A>G NP_001308895.1:p.Thr298=
NR_073525.3:n.1466A>G
NR_135905.2:n.1455A>G
NR_135906.2:n.896A>G
NR_135907.2:n.1142A>G
NR_135908.2:n.836A>G
NR_135909.2:n.1352A>G
NR_135910.2:n.1702A>G
NR_135911.2:n.1822A>G
NR_135912.2:n.2381A>G
NR_135913.2:n.2068A>G