Canonical Allele Identifier: CA2688632742

Gene: DNAAF11

Linked Data

• gnomAD v4: 8-132632676-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632680_132632681del , CM000670.2:g.132632680_132632681del	GRCh38
NC_000008.10:g.133644926_133644927del , CM000670.1:g.133644926_133644927del	GRCh37
NC_000008.9:g.133714108_133714109del	NCBI36
NG_033068.1:g.47940_47941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.653+62_653+63del MANE Select	ENSP00000484634.1:n.653+62_653+63del
ENST00000250173.5:c.653+62_653+63del	ENSP00000250173.2:n.653+62_653+63del
ENST00000518642.5:c.653+62_653+63del	ENSP00000428610.1:n.653+62_653+63del
ENST00000519595.5:c.653+62_653+63del	ENSP00000429791.1:n.653+62_653+63del
ENST00000520446.5:n.528+5257_528+5258del
ENST00000523503.1:n.415+5257_415+5258del
ENST00000618342.1:c.653+62_653+63del	ENSP00000484802.1:n.653+62_653+63del
ENST00000620350.4:c.653+62_653+63del	ENSP00000484634.1:n.653+62_653+63del
NM_012472.4:c.653+62_653+63del	NP_036604.2:n.653+62_653+63del
NR_073525.1:n.777+62_777+63del
XM_006716538.2:c.671+62_671+63del	XP_006716601.2:n.671+62_671+63del
XM_011516950.1:c.671+62_671+63del	XP_011515252.1:n.671+62_671+63del
XM_011516951.1:c.671+62_671+63del	XP_011515253.1:n.671+62_671+63del
XM_011516952.1:c.407+62_407+63del	XP_011515254.1:n.407+62_407+63del
XM_011516953.1:c.293+62_293+63del	XP_011515255.1:n.293+62_293+63del
XM_011516954.1:c.293+62_293+63del	XP_011515256.1:n.293+62_293+63del
XR_428377.2:n.796+62_796+63del
NM_001321961.1:c.653+62_653+63del	NP_001308890.1:n.653+62_653+63del
NM_001321962.1:c.407+62_407+63del	NP_001308891.1:n.407+62_407+63del
NM_001321963.1:c.293+62_293+63del	NP_001308892.1:n.293+62_293+63del
NM_001321964.1:c.293+62_293+63del	NP_001308893.1:n.293+62_293+63del
NM_001321965.1:c.293+62_293+63del	NP_001308894.1:n.293+62_293+63del
NM_001321966.1:c.293+62_293+63del	NP_001308895.1:n.293+62_293+63del
NM_012472.5:c.653+62_653+63del	NP_036604.2:n.653+62_653+63del
NR_073525.2:n.777+62_777+63del
NR_135905.1:n.866+5257_866+5258del
NR_135906.1:n.307+5257_307+5258del
NR_135907.1:n.553+5257_553+5258del
NR_135908.1:n.307+5257_307+5258del
NR_135909.1:n.671+5257_671+5258del
NR_135910.1:n.978+5257_978+5258del
NR_135911.1:n.1057+5257_1057+5258del
NR_135912.1:n.1616+5257_1616+5258del
NR_135913.1:n.1303+5257_1303+5258del
XM_006716538.3:c.671+62_671+63del	XP_006716601.2:n.671+62_671+63del
XM_011516950.2:c.671+62_671+63del	XP_011515252.1:n.671+62_671+63del
XM_017013296.1:c.551+62_551+63del	XP_016868785.1:n.551+62_551+63del
XM_017013297.1:c.293+62_293+63del	XP_016868786.1:n.293+62_293+63del
XM_017013298.1:c.293+62_293+63del	XP_016868787.1:n.293+62_293+63del
NM_012472.6:c.653+62_653+63del MANE Select	NP_036604.2:n.653+62_653+63del
NM_001321961.2:c.653+62_653+63del	NP_001308890.1:n.653+62_653+63del
NM_001321962.2:c.407+62_407+63del	NP_001308891.1:n.407+62_407+63del
NM_001321963.2:c.293+62_293+63del	NP_001308892.1:n.293+62_293+63del
NM_001321964.2:c.293+62_293+63del	NP_001308893.1:n.293+62_293+63del
NM_001321965.2:c.293+62_293+63del	NP_001308894.1:n.293+62_293+63del
NM_001321966.2:c.293+62_293+63del	NP_001308895.1:n.293+62_293+63del
NR_073525.3:n.705+62_705+63del
NR_135905.2:n.794+5257_794+5258del
NR_135906.2:n.235+5257_235+5258del
NR_135907.2:n.481+5257_481+5258del
NR_135908.2:n.235+5257_235+5258del
NR_135909.2:n.691+5257_691+5258del
NR_135910.2:n.1041+5257_1041+5258del
NR_135911.2:n.1161+5257_1161+5258del
NR_135912.2:n.1720+5257_1720+5258del
NR_135913.2:n.1407+5257_1407+5258del