Canonical Allele Identifier: CA1820845773

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572407_132572408delinsCT , CM000670.2:g.132572407_132572408delinsCT	GRCh38
NC_000008.10:g.133584655_133584656delinsCT , CM000670.1:g.133584655_133584656delinsCT	GRCh37
NC_000008.9:g.133653837_133653838delinsCT	NCBI36
NG_033068.1:g.108208_108209delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1299_1300delinsAG MANE Select	ENSP00000484634.1:p.Gln433=
ENST00000250173.5:c.*163_*164delinsAG	ENSP00000250173.2:n.*163_*164delinsAG
ENST00000518642.5:c.*163_*164delinsAG	ENSP00000428610.1:n.*163_*164delinsAG
ENST00000519595.5:c.1299_1300delinsAG	ENSP00000429791.1:p.Gln433=
ENST00000522789.5:c.519_520delinsAG	ENSP00000428015.1:p.Gln173=
ENST00000618342.1:c.1299_1300delinsAG	ENSP00000484802.1:p.Gln433=
ENST00000620350.4:c.1299_1300delinsAG	ENSP00000484634.1:p.Gln433=
NM_012472.4:c.1299_1300delinsAG	NP_036604.2:p.Gln433=
NR_073525.1:n.1523_1524delinsAG
XM_006716538.2:c.1317_1318delinsAG	XP_006716601.2:p.Gln439=
XM_011516950.1:c.1257_1258delinsAG	XP_011515252.1:p.Gln419=
XM_011516952.1:c.1053_1054delinsAG	XP_011515254.1:p.Gln351=
XM_011516953.1:c.939_940delinsAG	XP_011515255.1:p.Gln313=
XM_011516954.1:c.939_940delinsAG	XP_011515256.1:p.Gln313=
XR_428377.2:n.1551_1552delinsAG
NM_001321961.1:c.1239_1240delinsAG	NP_001308890.1:p.Gln413=
NM_001321962.1:c.1053_1054delinsAG	NP_001308891.1:p.Gln351=
NM_001321963.1:c.939_940delinsAG	NP_001308892.1:p.Gln313=
NM_001321964.1:c.939_940delinsAG	NP_001308893.1:p.Gln313=
NM_001321965.1:c.939_940delinsAG	NP_001308894.1:p.Gln313=
NM_001321966.1:c.879_880delinsAG	NP_001308895.1:p.Gln293=
NM_012472.5:c.1299_1300delinsAG	NP_036604.2:p.Gln433=
NR_073525.2:n.1523_1524delinsAG
NR_135905.1:n.1512_1513delinsAG
NR_135906.1:n.953_954delinsAG
NR_135907.1:n.1199_1200delinsAG
NR_135908.1:n.893_894delinsAG
NR_135909.1:n.1317_1318delinsAG
NR_135910.1:n.1624_1625delinsAG
NR_135911.1:n.1703_1704delinsAG
NR_135912.1:n.2262_2263delinsAG
NR_135913.1:n.1949_1950delinsAG
XM_006716538.3:c.1317_1318delinsAG	XP_006716601.2:p.Gln439=
XM_011516950.2:c.1257_1258delinsAG	XP_011515252.1:p.Gln419=
XM_017013296.1:c.1197_1198delinsAG	XP_016868785.1:p.Gln399=
XM_017013297.1:c.939_940delinsAG	XP_016868786.1:p.Gln313=
XM_017013298.1:c.939_940delinsAG	XP_016868787.1:p.Gln313=
NM_012472.6:c.1299_1300delinsAG MANE Select	NP_036604.2:p.Gln433=
NM_001321961.2:c.1239_1240delinsAG	NP_001308890.1:p.Gln413=
NM_001321962.2:c.1053_1054delinsAG	NP_001308891.1:p.Gln351=
NM_001321963.2:c.939_940delinsAG	NP_001308892.1:p.Gln313=
NM_001321964.2:c.939_940delinsAG	NP_001308893.1:p.Gln313=
NM_001321965.2:c.939_940delinsAG	NP_001308894.1:p.Gln313=
NM_001321966.2:c.879_880delinsAG	NP_001308895.1:p.Gln293=
NR_073525.3:n.1451_1452delinsAG
NR_135905.2:n.1440_1441delinsAG
NR_135906.2:n.881_882delinsAG
NR_135907.2:n.1127_1128delinsAG
NR_135908.2:n.821_822delinsAG
NR_135909.2:n.1337_1338delinsAG
NR_135910.2:n.1687_1688delinsAG
NR_135911.2:n.1807_1808delinsAG
NR_135912.2:n.2366_2367delinsAG
NR_135913.2:n.2053_2054delinsAG