Canonical Allele Identifier: CA1820870595
Gene: DNAAF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132632750T= , CM000670.2:g.132632750T= GRCh38
NC_000008.10:g.133644996T= , CM000670.1:g.133644996T= GRCh37
NC_000008.9:g.133714178T= NCBI36
NG_033068.1:g.47868A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000620350.5:c.643A= MANE Select ENSP00000484634.1:p.Asn215=
ENST00000250173.5:c.643A= ENSP00000250173.2:p.Asn215=
ENST00000518642.5:c.643A= ENSP00000428610.1:p.Asn215=
ENST00000519595.5:c.643A= ENSP00000429791.1:p.Asn215=
ENST00000520446.5:n.528+5185A=
ENST00000523503.1:n.415+5185A=
ENST00000618342.1:c.643A= ENSP00000484802.1:p.Asn215=
ENST00000620350.4:c.643A= ENSP00000484634.1:p.Asn215=
NM_012472.4:c.643A= NP_036604.2:p.Asn215=
NR_073525.1:n.767A=
XM_006716538.2:c.661A= XP_006716601.2:p.Asn221=
XM_011516950.1:c.661A= XP_011515252.1:p.Asn221=
XM_011516951.1:c.661A= XP_011515253.1:p.Asn221=
XM_011516952.1:c.397A= XP_011515254.1:p.Asn133=
XM_011516953.1:c.283A= XP_011515255.1:p.Asn95=
XM_011516954.1:c.283A= XP_011515256.1:p.Asn95=
XR_428377.2:n.786A=
NM_001321961.1:c.643A= NP_001308890.1:p.Asn215=
NM_001321962.1:c.397A= NP_001308891.1:p.Asn133=
NM_001321963.1:c.283A= NP_001308892.1:p.Asn95=
NM_001321964.1:c.283A= NP_001308893.1:p.Asn95=
NM_001321965.1:c.283A= NP_001308894.1:p.Asn95=
NM_001321966.1:c.283A= NP_001308895.1:p.Asn95=
NM_012472.5:c.643A= NP_036604.2:p.Asn215=
NR_073525.2:n.767A=
NR_135905.1:n.866+5185A=
NR_135906.1:n.307+5185A=
NR_135907.1:n.553+5185A=
NR_135908.1:n.307+5185A=
NR_135909.1:n.671+5185A=
NR_135910.1:n.978+5185A=
NR_135911.1:n.1057+5185A=
NR_135912.1:n.1616+5185A=
NR_135913.1:n.1303+5185A=
XM_006716538.3:c.661A= XP_006716601.2:p.Asn221=
XM_011516950.2:c.661A= XP_011515252.1:p.Asn221=
XM_017013296.1:c.541A= XP_016868785.1:p.Asn181=
XM_017013297.1:c.283A= XP_016868786.1:p.Asn95=
XM_017013298.1:c.283A= XP_016868787.1:p.Asn95=
NM_012472.6:c.643A= MANE Select NP_036604.2:p.Asn215=
NM_001321961.2:c.643A= NP_001308890.1:p.Asn215=
NM_001321962.2:c.397A= NP_001308891.1:p.Asn133=
NM_001321963.2:c.283A= NP_001308892.1:p.Asn95=
NM_001321964.2:c.283A= NP_001308893.1:p.Asn95=
NM_001321965.2:c.283A= NP_001308894.1:p.Asn95=
NM_001321966.2:c.283A= NP_001308895.1:p.Asn95=
NR_073525.3:n.695A=
NR_135905.2:n.794+5185A=
NR_135906.2:n.235+5185A=
NR_135907.2:n.481+5185A=
NR_135908.2:n.235+5185A=
NR_135909.2:n.691+5185A=
NR_135910.2:n.1041+5185A=
NR_135911.2:n.1161+5185A=
NR_135912.2:n.1720+5185A=
NR_135913.2:n.1407+5185A=