Canonical Allele Identifier: CA1119375977

Gene: DNAAF11

Linked Data

• gnomAD v3: 8-132632512-CAAATT-C
• gnomAD v4: 8-132632512-CAAATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632516_132632520del , CM000670.2:g.132632516_132632520del	GRCh38
NC_000008.10:g.133644762_133644766del , CM000670.1:g.133644762_133644766del	GRCh37
NC_000008.9:g.133713944_133713948del	NCBI36
NG_033068.1:g.48101_48105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.653+223_653+227del MANE Select	ENSP00000484634.1:n.653+223_653+227del
ENST00000250173.5:c.653+223_653+227del	ENSP00000250173.2:n.653+223_653+227del
ENST00000518642.5:c.653+223_653+227del	ENSP00000428610.1:n.653+223_653+227del
ENST00000519595.5:c.653+223_653+227del	ENSP00000429791.1:n.653+223_653+227del
ENST00000520446.5:n.528+5418_528+5422del
ENST00000523503.1:n.415+5418_415+5422del
ENST00000618342.1:c.653+223_653+227del	ENSP00000484802.1:n.653+223_653+227del
ENST00000620350.4:c.653+223_653+227del	ENSP00000484634.1:n.653+223_653+227del
NM_012472.4:c.653+223_653+227del	NP_036604.2:n.653+223_653+227del
NR_073525.1:n.777+223_777+227del
XM_006716538.2:c.671+223_671+227del	XP_006716601.2:n.671+223_671+227del
XM_011516950.1:c.671+223_671+227del	XP_011515252.1:n.671+223_671+227del
XM_011516951.1:c.671+223_671+227del	XP_011515253.1:n.671+223_671+227del
XM_011516952.1:c.407+223_407+227del	XP_011515254.1:n.407+223_407+227del
XM_011516953.1:c.293+223_293+227del	XP_011515255.1:n.293+223_293+227del
XM_011516954.1:c.293+223_293+227del	XP_011515256.1:n.293+223_293+227del
XR_428377.2:n.796+223_796+227del
NM_001321961.1:c.653+223_653+227del	NP_001308890.1:n.653+223_653+227del
NM_001321962.1:c.407+223_407+227del	NP_001308891.1:n.407+223_407+227del
NM_001321963.1:c.293+223_293+227del	NP_001308892.1:n.293+223_293+227del
NM_001321964.1:c.293+223_293+227del	NP_001308893.1:n.293+223_293+227del
NM_001321965.1:c.293+223_293+227del	NP_001308894.1:n.293+223_293+227del
NM_001321966.1:c.293+223_293+227del	NP_001308895.1:n.293+223_293+227del
NM_012472.5:c.653+223_653+227del	NP_036604.2:n.653+223_653+227del
NR_073525.2:n.777+223_777+227del
NR_135905.1:n.866+5418_866+5422del
NR_135906.1:n.307+5418_307+5422del
NR_135907.1:n.553+5418_553+5422del
NR_135908.1:n.307+5418_307+5422del
NR_135909.1:n.671+5418_671+5422del
NR_135910.1:n.978+5418_978+5422del
NR_135911.1:n.1057+5418_1057+5422del
NR_135912.1:n.1616+5418_1616+5422del
NR_135913.1:n.1303+5418_1303+5422del
XM_006716538.3:c.671+223_671+227del	XP_006716601.2:n.671+223_671+227del
XM_011516950.2:c.671+223_671+227del	XP_011515252.1:n.671+223_671+227del
XM_017013296.1:c.551+223_551+227del	XP_016868785.1:n.551+223_551+227del
XM_017013297.1:c.293+223_293+227del	XP_016868786.1:n.293+223_293+227del
XM_017013298.1:c.293+223_293+227del	XP_016868787.1:n.293+223_293+227del
NM_012472.6:c.653+223_653+227del MANE Select	NP_036604.2:n.653+223_653+227del
NM_001321961.2:c.653+223_653+227del	NP_001308890.1:n.653+223_653+227del
NM_001321962.2:c.407+223_407+227del	NP_001308891.1:n.407+223_407+227del
NM_001321963.2:c.293+223_293+227del	NP_001308892.1:n.293+223_293+227del
NM_001321964.2:c.293+223_293+227del	NP_001308893.1:n.293+223_293+227del
NM_001321965.2:c.293+223_293+227del	NP_001308894.1:n.293+223_293+227del
NM_001321966.2:c.293+223_293+227del	NP_001308895.1:n.293+223_293+227del
NR_073525.3:n.705+223_705+227del
NR_135905.2:n.794+5418_794+5422del
NR_135906.2:n.235+5418_235+5422del
NR_135907.2:n.481+5418_481+5422del
NR_135908.2:n.235+5418_235+5422del
NR_135909.2:n.691+5418_691+5422del
NR_135910.2:n.1041+5418_1041+5422del
NR_135911.2:n.1161+5418_1161+5422del
NR_135912.2:n.1720+5418_1720+5422del
NR_135913.2:n.1407+5418_1407+5422del