Canonical Allele Identifier: CA1820870809

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632865_132632866delinsGT , CM000670.2:g.132632865_132632866delinsGT	GRCh38
NC_000008.10:g.133645111_133645112delinsGT , CM000670.1:g.133645111_133645112delinsGT	GRCh37
NC_000008.9:g.133714293_133714294delinsGT	NCBI36
NG_033068.1:g.47752_47753delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000620350.5:c.527_528delinsAC MANE Select	ENSP00000484634.1:p.His176=
ENST00000250173.5:c.527_528delinsAC	ENSP00000250173.2:p.His176=
ENST00000518642.5:c.527_528delinsAC	ENSP00000428610.1:p.His176=
ENST00000519595.5:c.527_528delinsAC	ENSP00000429791.1:p.His176=
ENST00000520446.5:n.528+5069_528+5070delinsAC
ENST00000523503.1:n.415+5069_415+5070delinsAC
ENST00000618342.1:c.527_528delinsAC	ENSP00000484802.1:p.His176=
ENST00000620350.4:c.527_528delinsAC	ENSP00000484634.1:p.His176=
NM_012472.4:c.527_528delinsAC	NP_036604.2:p.His176=
NR_073525.1:n.651_652delinsAC
XM_006716538.2:c.545_546delinsAC	XP_006716601.2:p.His182=
XM_011516950.1:c.545_546delinsAC	XP_011515252.1:p.His182=
XM_011516951.1:c.545_546delinsAC	XP_011515253.1:p.His182=
XM_011516952.1:c.281_282delinsAC	XP_011515254.1:p.His94=
XM_011516953.1:c.167_168delinsAC	XP_011515255.1:p.His56=
XM_011516954.1:c.167_168delinsAC	XP_011515256.1:p.His56=
XR_428377.2:n.670_671delinsAC
NM_001321961.1:c.527_528delinsAC	NP_001308890.1:p.His176=
NM_001321962.1:c.281_282delinsAC	NP_001308891.1:p.His94=
NM_001321963.1:c.167_168delinsAC	NP_001308892.1:p.His56=
NM_001321964.1:c.167_168delinsAC	NP_001308893.1:p.His56=
NM_001321965.1:c.167_168delinsAC	NP_001308894.1:p.His56=
NM_001321966.1:c.167_168delinsAC	NP_001308895.1:p.His56=
NM_012472.5:c.527_528delinsAC	NP_036604.2:p.His176=
NR_073525.2:n.651_652delinsAC
NR_135905.1:n.866+5069_866+5070delinsAC
NR_135906.1:n.307+5069_307+5070delinsAC
NR_135907.1:n.553+5069_553+5070delinsAC
NR_135908.1:n.307+5069_307+5070delinsAC
NR_135909.1:n.671+5069_671+5070delinsAC
NR_135910.1:n.978+5069_978+5070delinsAC
NR_135911.1:n.1057+5069_1057+5070delinsAC
NR_135912.1:n.1616+5069_1616+5070delinsAC
NR_135913.1:n.1303+5069_1303+5070delinsAC
XM_006716538.3:c.545_546delinsAC	XP_006716601.2:p.His182=
XM_011516950.2:c.545_546delinsAC	XP_011515252.1:p.His182=
XM_017013296.1:c.425_426delinsAC	XP_016868785.1:p.His142=
XM_017013297.1:c.167_168delinsAC	XP_016868786.1:p.His56=
XM_017013298.1:c.167_168delinsAC	XP_016868787.1:p.His56=
NM_012472.6:c.527_528delinsAC MANE Select	NP_036604.2:p.His176=
NM_001321961.2:c.527_528delinsAC	NP_001308890.1:p.His176=
NM_001321962.2:c.281_282delinsAC	NP_001308891.1:p.His94=
NM_001321963.2:c.167_168delinsAC	NP_001308892.1:p.His56=
NM_001321964.2:c.167_168delinsAC	NP_001308893.1:p.His56=
NM_001321965.2:c.167_168delinsAC	NP_001308894.1:p.His56=
NM_001321966.2:c.167_168delinsAC	NP_001308895.1:p.His56=
NR_073525.3:n.579_580delinsAC
NR_135905.2:n.794+5069_794+5070delinsAC
NR_135906.2:n.235+5069_235+5070delinsAC
NR_135907.2:n.481+5069_481+5070delinsAC
NR_135908.2:n.235+5069_235+5070delinsAC
NR_135909.2:n.691+5069_691+5070delinsAC
NR_135910.2:n.1041+5069_1041+5070delinsAC
NR_135911.2:n.1161+5069_1161+5070delinsAC
NR_135912.2:n.1720+5069_1720+5070delinsAC
NR_135913.2:n.1407+5069_1407+5070delinsAC