Canonical Allele Identifier: CA1820845617

Gene: DNAAF11

Linked Data

• dbSNP Id: rs1814246743

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572079_132572084del , CM000670.2:g.132572079_132572084del	GRCh38
NC_000008.10:g.133584327_133584332del , CM000670.1:g.133584327_133584332del	GRCh37
NC_000008.9:g.133653509_133653514del	NCBI36
NG_033068.1:g.108535_108540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*225_*230del MANE Select	ENSP00000484634.1:n.*225_*230del
ENST00000519595.5:c.*225_*230del	ENSP00000429791.1:n.*225_*230del
ENST00000618342.1:c.1626_1631del	ENSP00000484802.1:n.1626_1631del
ENST00000620350.4:c.*225_*230del	ENSP00000484634.1:n.*225_*230del
NM_012472.4:c.*225_*230del	NP_036604.2:n.*225_*230del
NR_073525.1:n.1850_1855del
XM_006716538.2:c.*225_*230del	XP_006716601.2:n.*225_*230del
XM_011516950.1:c.*225_*230del	XP_011515252.1:n.*225_*230del
XM_011516952.1:c.*225_*230del	XP_011515254.1:n.*225_*230del
XM_011516953.1:c.*225_*230del	XP_011515255.1:n.*225_*230del
XM_011516954.1:c.*225_*230del	XP_011515256.1:n.*225_*230del
XR_428377.2:n.1878_1883del
NM_001321961.1:c.*225_*230del	NP_001308890.1:n.*225_*230del
NM_001321962.1:c.*225_*230del	NP_001308891.1:n.*225_*230del
NM_001321963.1:c.*225_*230del	NP_001308892.1:n.*225_*230del
NM_001321964.1:c.*225_*230del	NP_001308893.1:n.*225_*230del
NM_001321965.1:c.*225_*230del	NP_001308894.1:n.*225_*230del
NM_001321966.1:c.*225_*230del	NP_001308895.1:n.*225_*230del
NM_012472.5:c.*225_*230del	NP_036604.2:n.*225_*230del
NR_073525.2:n.1850_1855del
NR_135905.1:n.1839_1844del
NR_135906.1:n.1280_1285del
NR_135907.1:n.1526_1531del
NR_135908.1:n.1220_1225del
NR_135909.1:n.1644_1649del
NR_135910.1:n.1951_1956del
NR_135911.1:n.2030_2035del
NR_135912.1:n.2589_2594del
NR_135913.1:n.2276_2281del
XM_006716538.3:c.*225_*230del	XP_006716601.2:n.*225_*230del
XM_011516950.2:c.*225_*230del	XP_011515252.1:n.*225_*230del
XM_017013296.1:c.*225_*230del	XP_016868785.1:n.*225_*230del
XM_017013297.1:c.*225_*230del	XP_016868786.1:n.*225_*230del
XM_017013298.1:c.*225_*230del	XP_016868787.1:n.*225_*230del
NM_012472.6:c.*225_*230del MANE Select	NP_036604.2:n.*225_*230del
NM_001321961.2:c.*225_*230del	NP_001308890.1:n.*225_*230del
NM_001321962.2:c.*225_*230del	NP_001308891.1:n.*225_*230del
NM_001321963.2:c.*225_*230del	NP_001308892.1:n.*225_*230del
NM_001321964.2:c.*225_*230del	NP_001308893.1:n.*225_*230del
NM_001321965.2:c.*225_*230del	NP_001308894.1:n.*225_*230del
NM_001321966.2:c.*225_*230del	NP_001308895.1:n.*225_*230del
NR_073525.3:n.1778_1783del
NR_135905.2:n.1767_1772del
NR_135906.2:n.1208_1213del
NR_135907.2:n.1454_1459del
NR_135908.2:n.1148_1153del
NR_135909.2:n.1664_1669del
NR_135910.2:n.2014_2019del
NR_135911.2:n.2134_2139del
NR_135912.2:n.2693_2698del
NR_135913.2:n.2380_2385del