Canonical Allele Identifier: CA2515963824

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572175_132572176insTAAAA , CM000670.2:g.132572175_132572176insTAAAA	GRCh38
NC_000008.10:g.133584423_133584424insTAAAA , CM000670.1:g.133584423_133584424insTAAAA	GRCh37
NC_000008.9:g.133653605_133653606insTAAAA	NCBI36
NG_033068.1:g.108441_108442insTTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*131_*132insTTTAT MANE Select	ENSP00000484634.1:n.*131_*132insTTTAT
ENST00000519595.5:c.*131_*132insTTTAT	ENSP00000429791.1:n.*131_*132insTTTAT
ENST00000618342.1:c.1532_1533insTTTAT	ENSP00000484802.1:n.1532_1533insTTTAT
ENST00000620350.4:c.*131_*132insTTTAT	ENSP00000484634.1:n.*131_*132insTTTAT
NM_012472.4:c.*131_*132insTTTAT	NP_036604.2:n.*131_*132insTTTAT
NR_073525.1:n.1756_1757insTTTAT
XM_006716538.2:c.*131_*132insTTTAT	XP_006716601.2:n.*131_*132insTTTAT
XM_011516950.1:c.*131_*132insTTTAT	XP_011515252.1:n.*131_*132insTTTAT
XM_011516952.1:c.*131_*132insTTTAT	XP_011515254.1:n.*131_*132insTTTAT
XM_011516953.1:c.*131_*132insTTTAT	XP_011515255.1:n.*131_*132insTTTAT
XM_011516954.1:c.*131_*132insTTTAT	XP_011515256.1:n.*131_*132insTTTAT
XR_428377.2:n.1784_1785insTTTAT
NM_001321961.1:c.*131_*132insTTTAT	NP_001308890.1:n.*131_*132insTTTAT
NM_001321962.1:c.*131_*132insTTTAT	NP_001308891.1:n.*131_*132insTTTAT
NM_001321963.1:c.*131_*132insTTTAT	NP_001308892.1:n.*131_*132insTTTAT
NM_001321964.1:c.*131_*132insTTTAT	NP_001308893.1:n.*131_*132insTTTAT
NM_001321965.1:c.*131_*132insTTTAT	NP_001308894.1:n.*131_*132insTTTAT
NM_001321966.1:c.*131_*132insTTTAT	NP_001308895.1:n.*131_*132insTTTAT
NM_012472.5:c.*131_*132insTTTAT	NP_036604.2:n.*131_*132insTTTAT
NR_073525.2:n.1756_1757insTTTAT
NR_135905.1:n.1745_1746insTTTAT
NR_135906.1:n.1186_1187insTTTAT
NR_135907.1:n.1432_1433insTTTAT
NR_135908.1:n.1126_1127insTTTAT
NR_135909.1:n.1550_1551insTTTAT
NR_135910.1:n.1857_1858insTTTAT
NR_135911.1:n.1936_1937insTTTAT
NR_135912.1:n.2495_2496insTTTAT
NR_135913.1:n.2182_2183insTTTAT
XM_006716538.3:c.*131_*132insTTTAT	XP_006716601.2:n.*131_*132insTTTAT
XM_011516950.2:c.*131_*132insTTTAT	XP_011515252.1:n.*131_*132insTTTAT
XM_017013296.1:c.*131_*132insTTTAT	XP_016868785.1:n.*131_*132insTTTAT
XM_017013297.1:c.*131_*132insTTTAT	XP_016868786.1:n.*131_*132insTTTAT
XM_017013298.1:c.*131_*132insTTTAT	XP_016868787.1:n.*131_*132insTTTAT
NM_012472.6:c.*131_*132insTTTAT MANE Select	NP_036604.2:n.*131_*132insTTTAT
NM_001321961.2:c.*131_*132insTTTAT	NP_001308890.1:n.*131_*132insTTTAT
NM_001321962.2:c.*131_*132insTTTAT	NP_001308891.1:n.*131_*132insTTTAT
NM_001321963.2:c.*131_*132insTTTAT	NP_001308892.1:n.*131_*132insTTTAT
NM_001321964.2:c.*131_*132insTTTAT	NP_001308893.1:n.*131_*132insTTTAT
NM_001321965.2:c.*131_*132insTTTAT	NP_001308894.1:n.*131_*132insTTTAT
NM_001321966.2:c.*131_*132insTTTAT	NP_001308895.1:n.*131_*132insTTTAT
NR_073525.3:n.1684_1685insTTTAT
NR_135905.2:n.1673_1674insTTTAT
NR_135906.2:n.1114_1115insTTTAT
NR_135907.2:n.1360_1361insTTTAT
NR_135908.2:n.1054_1055insTTTAT
NR_135909.2:n.1570_1571insTTTAT
NR_135910.2:n.1920_1921insTTTAT
NR_135911.2:n.2040_2041insTTTAT
NR_135912.2:n.2599_2600insTTTAT
NR_135913.2:n.2286_2287insTTTAT