Canonical Allele Identifier: CA1820845642

Gene: DNAAF11

Linked Data

• dbSNP Id: rs1814253020

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572137_132572142del , CM000670.2:g.132572137_132572142del	GRCh38
NC_000008.10:g.133584385_133584390del , CM000670.1:g.133584385_133584390del	GRCh37
NC_000008.9:g.133653567_133653572del	NCBI36
NG_033068.1:g.108481_108486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*171_*176del MANE Select	ENSP00000484634.1:n.*171_*176del
ENST00000519595.5:c.*171_*176del	ENSP00000429791.1:n.*171_*176del
ENST00000618342.1:c.1572_1577del	ENSP00000484802.1:n.1572_1577del
ENST00000620350.4:c.*171_*176del	ENSP00000484634.1:n.*171_*176del
NM_012472.4:c.*171_*176del	NP_036604.2:n.*171_*176del
NR_073525.1:n.1796_1801del
XM_006716538.2:c.*171_*176del	XP_006716601.2:n.*171_*176del
XM_011516950.1:c.*171_*176del	XP_011515252.1:n.*171_*176del
XM_011516952.1:c.*171_*176del	XP_011515254.1:n.*171_*176del
XM_011516953.1:c.*171_*176del	XP_011515255.1:n.*171_*176del
XM_011516954.1:c.*171_*176del	XP_011515256.1:n.*171_*176del
XR_428377.2:n.1824_1829del
NM_001321961.1:c.*171_*176del	NP_001308890.1:n.*171_*176del
NM_001321962.1:c.*171_*176del	NP_001308891.1:n.*171_*176del
NM_001321963.1:c.*171_*176del	NP_001308892.1:n.*171_*176del
NM_001321964.1:c.*171_*176del	NP_001308893.1:n.*171_*176del
NM_001321965.1:c.*171_*176del	NP_001308894.1:n.*171_*176del
NM_001321966.1:c.*171_*176del	NP_001308895.1:n.*171_*176del
NM_012472.5:c.*171_*176del	NP_036604.2:n.*171_*176del
NR_073525.2:n.1796_1801del
NR_135905.1:n.1785_1790del
NR_135906.1:n.1226_1231del
NR_135907.1:n.1472_1477del
NR_135908.1:n.1166_1171del
NR_135909.1:n.1590_1595del
NR_135910.1:n.1897_1902del
NR_135911.1:n.1976_1981del
NR_135912.1:n.2535_2540del
NR_135913.1:n.2222_2227del
XM_006716538.3:c.*171_*176del	XP_006716601.2:n.*171_*176del
XM_011516950.2:c.*171_*176del	XP_011515252.1:n.*171_*176del
XM_017013296.1:c.*171_*176del	XP_016868785.1:n.*171_*176del
XM_017013297.1:c.*171_*176del	XP_016868786.1:n.*171_*176del
XM_017013298.1:c.*171_*176del	XP_016868787.1:n.*171_*176del
NM_012472.6:c.*171_*176del MANE Select	NP_036604.2:n.*171_*176del
NM_001321961.2:c.*171_*176del	NP_001308890.1:n.*171_*176del
NM_001321962.2:c.*171_*176del	NP_001308891.1:n.*171_*176del
NM_001321963.2:c.*171_*176del	NP_001308892.1:n.*171_*176del
NM_001321964.2:c.*171_*176del	NP_001308893.1:n.*171_*176del
NM_001321965.2:c.*171_*176del	NP_001308894.1:n.*171_*176del
NM_001321966.2:c.*171_*176del	NP_001308895.1:n.*171_*176del
NR_073525.3:n.1724_1729del
NR_135905.2:n.1713_1718del
NR_135906.2:n.1154_1159del
NR_135907.2:n.1400_1405del
NR_135908.2:n.1094_1099del
NR_135909.2:n.1610_1615del
NR_135910.2:n.1960_1965del
NR_135911.2:n.2080_2085del
NR_135912.2:n.2639_2644del
NR_135913.2:n.2326_2331del