Canonical Allele Identifier: CA1820870457

Gene: DNAAF11

Linked Data

• dbSNP Id: rs1820902493
• gnomAD v4: 8-132632594-TCATATTCTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632598_132632607del , CM000670.2:g.132632598_132632607del	GRCh38
NC_000008.10:g.133644844_133644853del , CM000670.1:g.133644844_133644853del	GRCh37
NC_000008.9:g.133714026_133714035del	NCBI36
NG_033068.1:g.48014_48023del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.653+136_653+145del MANE Select	ENSP00000484634.1:n.653+136_653+145del
ENST00000250173.5:c.653+136_653+145del	ENSP00000250173.2:n.653+136_653+145del
ENST00000518642.5:c.653+136_653+145del	ENSP00000428610.1:n.653+136_653+145del
ENST00000519595.5:c.653+136_653+145del	ENSP00000429791.1:n.653+136_653+145del
ENST00000520446.5:n.528+5331_528+5340del
ENST00000523503.1:n.415+5331_415+5340del
ENST00000618342.1:c.653+136_653+145del	ENSP00000484802.1:n.653+136_653+145del
ENST00000620350.4:c.653+136_653+145del	ENSP00000484634.1:n.653+136_653+145del
NM_012472.4:c.653+136_653+145del	NP_036604.2:n.653+136_653+145del
NR_073525.1:n.777+136_777+145del
XM_006716538.2:c.671+136_671+145del	XP_006716601.2:n.671+136_671+145del
XM_011516950.1:c.671+136_671+145del	XP_011515252.1:n.671+136_671+145del
XM_011516951.1:c.671+136_671+145del	XP_011515253.1:n.671+136_671+145del
XM_011516952.1:c.407+136_407+145del	XP_011515254.1:n.407+136_407+145del
XM_011516953.1:c.293+136_293+145del	XP_011515255.1:n.293+136_293+145del
XM_011516954.1:c.293+136_293+145del	XP_011515256.1:n.293+136_293+145del
XR_428377.2:n.796+136_796+145del
NM_001321961.1:c.653+136_653+145del	NP_001308890.1:n.653+136_653+145del
NM_001321962.1:c.407+136_407+145del	NP_001308891.1:n.407+136_407+145del
NM_001321963.1:c.293+136_293+145del	NP_001308892.1:n.293+136_293+145del
NM_001321964.1:c.293+136_293+145del	NP_001308893.1:n.293+136_293+145del
NM_001321965.1:c.293+136_293+145del	NP_001308894.1:n.293+136_293+145del
NM_001321966.1:c.293+136_293+145del	NP_001308895.1:n.293+136_293+145del
NM_012472.5:c.653+136_653+145del	NP_036604.2:n.653+136_653+145del
NR_073525.2:n.777+136_777+145del
NR_135905.1:n.866+5331_866+5340del
NR_135906.1:n.307+5331_307+5340del
NR_135907.1:n.553+5331_553+5340del
NR_135908.1:n.307+5331_307+5340del
NR_135909.1:n.671+5331_671+5340del
NR_135910.1:n.978+5331_978+5340del
NR_135911.1:n.1057+5331_1057+5340del
NR_135912.1:n.1616+5331_1616+5340del
NR_135913.1:n.1303+5331_1303+5340del
XM_006716538.3:c.671+136_671+145del	XP_006716601.2:n.671+136_671+145del
XM_011516950.2:c.671+136_671+145del	XP_011515252.1:n.671+136_671+145del
XM_017013296.1:c.551+136_551+145del	XP_016868785.1:n.551+136_551+145del
XM_017013297.1:c.293+136_293+145del	XP_016868786.1:n.293+136_293+145del
XM_017013298.1:c.293+136_293+145del	XP_016868787.1:n.293+136_293+145del
NM_012472.6:c.653+136_653+145del MANE Select	NP_036604.2:n.653+136_653+145del
NM_001321961.2:c.653+136_653+145del	NP_001308890.1:n.653+136_653+145del
NM_001321962.2:c.407+136_407+145del	NP_001308891.1:n.407+136_407+145del
NM_001321963.2:c.293+136_293+145del	NP_001308892.1:n.293+136_293+145del
NM_001321964.2:c.293+136_293+145del	NP_001308893.1:n.293+136_293+145del
NM_001321965.2:c.293+136_293+145del	NP_001308894.1:n.293+136_293+145del
NM_001321966.2:c.293+136_293+145del	NP_001308895.1:n.293+136_293+145del
NR_073525.3:n.705+136_705+145del
NR_135905.2:n.794+5331_794+5340del
NR_135906.2:n.235+5331_235+5340del
NR_135907.2:n.481+5331_481+5340del
NR_135908.2:n.235+5331_235+5340del
NR_135909.2:n.691+5331_691+5340del
NR_135910.2:n.1041+5331_1041+5340del
NR_135911.2:n.1161+5331_1161+5340del
NR_135912.2:n.1720+5331_1720+5340del
NR_135913.2:n.1407+5331_1407+5340del