Canonical Allele Identifier: CA1820845749
Gene: DNAAF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132572350C= , CM000670.2:g.132572350C= GRCh38
NC_000008.10:g.133584598C= , CM000670.1:g.133584598C= GRCh37
NC_000008.9:g.133653780C= NCBI36
NG_033068.1:g.108266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.1357G= MANE Select ENSP00000484634.1:p.Asp453=
ENST00000250173.5:c.*221G= ENSP00000250173.2:n.*221G=
ENST00000518642.5:c.*221G= ENSP00000428610.1:n.*221G=
ENST00000519595.5:c.1357G= ENSP00000429791.1:p.Asp453=
ENST00000522789.5:c.577G= ENSP00000428015.1:p.Asp193=
ENST00000618342.1:c.1357G= ENSP00000484802.1:p.Asp453=
ENST00000620350.4:c.1357G= ENSP00000484634.1:p.Asp453=
NM_012472.4:c.1357G= NP_036604.2:p.Asp453=
NR_073525.1:n.1581G=
XM_006716538.2:c.1375G= XP_006716601.2:p.Asp459=
XM_011516950.1:c.1315G= XP_011515252.1:p.Asp439=
XM_011516952.1:c.1111G= XP_011515254.1:p.Asp371=
XM_011516953.1:c.997G= XP_011515255.1:p.Asp333=
XM_011516954.1:c.997G= XP_011515256.1:p.Asp333=
XR_428377.2:n.1609G=
NM_001321961.1:c.1297G= NP_001308890.1:p.Asp433=
NM_001321962.1:c.1111G= NP_001308891.1:p.Asp371=
NM_001321963.1:c.997G= NP_001308892.1:p.Asp333=
NM_001321964.1:c.997G= NP_001308893.1:p.Asp333=
NM_001321965.1:c.997G= NP_001308894.1:p.Asp333=
NM_001321966.1:c.937G= NP_001308895.1:p.Asp313=
NM_012472.5:c.1357G= NP_036604.2:p.Asp453=
NR_073525.2:n.1581G=
NR_135905.1:n.1570G=
NR_135906.1:n.1011G=
NR_135907.1:n.1257G=
NR_135908.1:n.951G=
NR_135909.1:n.1375G=
NR_135910.1:n.1682G=
NR_135911.1:n.1761G=
NR_135912.1:n.2320G=
NR_135913.1:n.2007G=
XM_006716538.3:c.1375G= XP_006716601.2:p.Asp459=
XM_011516950.2:c.1315G= XP_011515252.1:p.Asp439=
XM_017013296.1:c.1255G= XP_016868785.1:p.Asp419=
XM_017013297.1:c.997G= XP_016868786.1:p.Asp333=
XM_017013298.1:c.997G= XP_016868787.1:p.Asp333=
NM_012472.6:c.1357G= MANE Select NP_036604.2:p.Asp453=
NM_001321961.2:c.1297G= NP_001308890.1:p.Asp433=
NM_001321962.2:c.1111G= NP_001308891.1:p.Asp371=
NM_001321963.2:c.997G= NP_001308892.1:p.Asp333=
NM_001321964.2:c.997G= NP_001308893.1:p.Asp333=
NM_001321965.2:c.997G= NP_001308894.1:p.Asp333=
NM_001321966.2:c.937G= NP_001308895.1:p.Asp313=
NR_073525.3:n.1509G=
NR_135905.2:n.1498G=
NR_135906.2:n.939G=
NR_135907.2:n.1185G=
NR_135908.2:n.879G=
NR_135909.2:n.1395G=
NR_135910.2:n.1745G=
NR_135911.2:n.1865G=
NR_135912.2:n.2424G=
NR_135913.2:n.2111G=