Canonical Allele Identifier: CA2688630990

Gene: DNAAF11

Linked Data

• gnomAD v4: 8-132572271-GTGGGTCTCAGCCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572275_132572288del , CM000670.2:g.132572275_132572288del	GRCh38
NC_000008.10:g.133584523_133584536del , CM000670.1:g.133584523_133584536del	GRCh37
NC_000008.9:g.133653705_133653718del	NCBI36
NG_033068.1:g.108331_108344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*21_*34del MANE Select	ENSP00000484634.1:n.*21_*34del
ENST00000250173.5:c.*286_*299del	ENSP00000250173.2:n.*286_*299del
ENST00000518642.5:c.*286_*299del	ENSP00000428610.1:n.*286_*299del
ENST00000519595.5:c.*21_*34del	ENSP00000429791.1:n.*21_*34del
ENST00000522789.5:c.642_655del	ENSP00000428015.1:n.642_655del
ENST00000618342.1:c.1422_1435del	ENSP00000484802.1:n.1422_1435del
ENST00000620350.4:c.*21_*34del	ENSP00000484634.1:n.*21_*34del
NM_012472.4:c.*21_*34del	NP_036604.2:n.*21_*34del
NR_073525.1:n.1646_1659del
XM_006716538.2:c.*21_*34del	XP_006716601.2:n.*21_*34del
XM_011516950.1:c.*21_*34del	XP_011515252.1:n.*21_*34del
XM_011516952.1:c.*21_*34del	XP_011515254.1:n.*21_*34del
XM_011516953.1:c.*21_*34del	XP_011515255.1:n.*21_*34del
XM_011516954.1:c.*21_*34del	XP_011515256.1:n.*21_*34del
XR_428377.2:n.1674_1687del
NM_001321961.1:c.*21_*34del	NP_001308890.1:n.*21_*34del
NM_001321962.1:c.*21_*34del	NP_001308891.1:n.*21_*34del
NM_001321963.1:c.*21_*34del	NP_001308892.1:n.*21_*34del
NM_001321964.1:c.*21_*34del	NP_001308893.1:n.*21_*34del
NM_001321965.1:c.*21_*34del	NP_001308894.1:n.*21_*34del
NM_001321966.1:c.*21_*34del	NP_001308895.1:n.*21_*34del
NM_012472.5:c.*21_*34del	NP_036604.2:n.*21_*34del
NR_073525.2:n.1646_1659del
NR_135905.1:n.1635_1648del
NR_135906.1:n.1076_1089del
NR_135907.1:n.1322_1335del
NR_135908.1:n.1016_1029del
NR_135909.1:n.1440_1453del
NR_135910.1:n.1747_1760del
NR_135911.1:n.1826_1839del
NR_135912.1:n.2385_2398del
NR_135913.1:n.2072_2085del
XM_006716538.3:c.*21_*34del	XP_006716601.2:n.*21_*34del
XM_011516950.2:c.*21_*34del	XP_011515252.1:n.*21_*34del
XM_017013296.1:c.*21_*34del	XP_016868785.1:n.*21_*34del
XM_017013297.1:c.*21_*34del	XP_016868786.1:n.*21_*34del
XM_017013298.1:c.*21_*34del	XP_016868787.1:n.*21_*34del
NM_012472.6:c.*21_*34del MANE Select	NP_036604.2:n.*21_*34del
NM_001321961.2:c.*21_*34del	NP_001308890.1:n.*21_*34del
NM_001321962.2:c.*21_*34del	NP_001308891.1:n.*21_*34del
NM_001321963.2:c.*21_*34del	NP_001308892.1:n.*21_*34del
NM_001321964.2:c.*21_*34del	NP_001308893.1:n.*21_*34del
NM_001321965.2:c.*21_*34del	NP_001308894.1:n.*21_*34del
NM_001321966.2:c.*21_*34del	NP_001308895.1:n.*21_*34del
NR_073525.3:n.1574_1587del
NR_135905.2:n.1563_1576del
NR_135906.2:n.1004_1017del
NR_135907.2:n.1250_1263del
NR_135908.2:n.944_957del
NR_135909.2:n.1460_1473del
NR_135910.2:n.1810_1823del
NR_135911.2:n.1930_1943del
NR_135912.2:n.2489_2502del
NR_135913.2:n.2176_2189del