Canonical Allele Identifier: CA1820845630

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572107_132572111delinsGAGTT , CM000670.2:g.132572107_132572111delinsGAGTT	GRCh38
NC_000008.10:g.133584355_133584359delinsGAGTT , CM000670.1:g.133584355_133584359delinsGAGTT	GRCh37
NC_000008.9:g.133653537_133653541delinsGAGTT	NCBI36
NG_033068.1:g.108505_108509delinsAACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*195_*199delinsAACTC MANE Select	ENSP00000484634.1:n.*195_*199delinsAACTC
ENST00000519595.5:c.*195_*199delinsAACTC	ENSP00000429791.1:n.*195_*199delinsAACTC
ENST00000618342.1:c.1596_1600delinsAACTC	ENSP00000484802.1:n.1596_1600delinsAACTC
ENST00000620350.4:c.*195_*199delinsAACTC	ENSP00000484634.1:n.*195_*199delinsAACTC
NM_012472.4:c.*195_*199delinsAACTC	NP_036604.2:n.*195_*199delinsAACTC
NR_073525.1:n.1820_1824delinsAACTC
XM_006716538.2:c.*195_*199delinsAACTC	XP_006716601.2:n.*195_*199delinsAACTC
XM_011516950.1:c.*195_*199delinsAACTC	XP_011515252.1:n.*195_*199delinsAACTC
XM_011516952.1:c.*195_*199delinsAACTC	XP_011515254.1:n.*195_*199delinsAACTC
XM_011516953.1:c.*195_*199delinsAACTC	XP_011515255.1:n.*195_*199delinsAACTC
XM_011516954.1:c.*195_*199delinsAACTC	XP_011515256.1:n.*195_*199delinsAACTC
XR_428377.2:n.1848_1852delinsAACTC
NM_001321961.1:c.*195_*199delinsAACTC	NP_001308890.1:n.*195_*199delinsAACTC
NM_001321962.1:c.*195_*199delinsAACTC	NP_001308891.1:n.*195_*199delinsAACTC
NM_001321963.1:c.*195_*199delinsAACTC	NP_001308892.1:n.*195_*199delinsAACTC
NM_001321964.1:c.*195_*199delinsAACTC	NP_001308893.1:n.*195_*199delinsAACTC
NM_001321965.1:c.*195_*199delinsAACTC	NP_001308894.1:n.*195_*199delinsAACTC
NM_001321966.1:c.*195_*199delinsAACTC	NP_001308895.1:n.*195_*199delinsAACTC
NM_012472.5:c.*195_*199delinsAACTC	NP_036604.2:n.*195_*199delinsAACTC
NR_073525.2:n.1820_1824delinsAACTC
NR_135905.1:n.1809_1813delinsAACTC
NR_135906.1:n.1250_1254delinsAACTC
NR_135907.1:n.1496_1500delinsAACTC
NR_135908.1:n.1190_1194delinsAACTC
NR_135909.1:n.1614_1618delinsAACTC
NR_135910.1:n.1921_1925delinsAACTC
NR_135911.1:n.2000_2004delinsAACTC
NR_135912.1:n.2559_2563delinsAACTC
NR_135913.1:n.2246_2250delinsAACTC
XM_006716538.3:c.*195_*199delinsAACTC	XP_006716601.2:n.*195_*199delinsAACTC
XM_011516950.2:c.*195_*199delinsAACTC	XP_011515252.1:n.*195_*199delinsAACTC
XM_017013296.1:c.*195_*199delinsAACTC	XP_016868785.1:n.*195_*199delinsAACTC
XM_017013297.1:c.*195_*199delinsAACTC	XP_016868786.1:n.*195_*199delinsAACTC
XM_017013298.1:c.*195_*199delinsAACTC	XP_016868787.1:n.*195_*199delinsAACTC
NM_012472.6:c.*195_*199delinsAACTC MANE Select	NP_036604.2:n.*195_*199delinsAACTC
NM_001321961.2:c.*195_*199delinsAACTC	NP_001308890.1:n.*195_*199delinsAACTC
NM_001321962.2:c.*195_*199delinsAACTC	NP_001308891.1:n.*195_*199delinsAACTC
NM_001321963.2:c.*195_*199delinsAACTC	NP_001308892.1:n.*195_*199delinsAACTC
NM_001321964.2:c.*195_*199delinsAACTC	NP_001308893.1:n.*195_*199delinsAACTC
NM_001321965.2:c.*195_*199delinsAACTC	NP_001308894.1:n.*195_*199delinsAACTC
NM_001321966.2:c.*195_*199delinsAACTC	NP_001308895.1:n.*195_*199delinsAACTC
NR_073525.3:n.1748_1752delinsAACTC
NR_135905.2:n.1737_1741delinsAACTC
NR_135906.2:n.1178_1182delinsAACTC
NR_135907.2:n.1424_1428delinsAACTC
NR_135908.2:n.1118_1122delinsAACTC
NR_135909.2:n.1634_1638delinsAACTC
NR_135910.2:n.1984_1988delinsAACTC
NR_135911.2:n.2104_2108delinsAACTC
NR_135912.2:n.2663_2667delinsAACTC
NR_135913.2:n.2350_2354delinsAACTC