Canonical Allele Identifier: CA2579252092

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572517_132572519del , CM000670.2:g.132572517_132572519del	GRCh38
NC_000008.10:g.133584765_133584767del , CM000670.1:g.133584765_133584767del	GRCh37
NC_000008.9:g.133653947_133653949del	NCBI36
NG_033068.1:g.108100_108102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1227-36_1227-34del MANE Select	ENSP00000484634.1:n.1227-36_1227-34del
ENST00000250173.5:c.*91-36_*91-34del	ENSP00000250173.2:n.*91-36_*91-34del
ENST00000518642.5:c.*91-36_*91-34del	ENSP00000428610.1:n.*91-36_*91-34del
ENST00000519595.5:c.1227-36_1227-34del	ENSP00000429791.1:n.1227-36_1227-34del
ENST00000522597.1:n.496-36_496-34del
ENST00000522789.5:c.447-36_447-34del	ENSP00000428015.1:n.447-36_447-34del
ENST00000618342.1:c.1227-36_1227-34del	ENSP00000484802.1:n.1227-36_1227-34del
ENST00000620350.4:c.1227-36_1227-34del	ENSP00000484634.1:n.1227-36_1227-34del
NM_012472.4:c.1227-36_1227-34del	NP_036604.2:n.1227-36_1227-34del
NR_073525.1:n.1451-36_1451-34del
XM_006716538.2:c.1245-36_1245-34del	XP_006716601.2:n.1245-36_1245-34del
XM_011516950.1:c.1185-36_1185-34del	XP_011515252.1:n.1185-36_1185-34del
XM_011516952.1:c.981-36_981-34del	XP_011515254.1:n.981-36_981-34del
XM_011516953.1:c.867-36_867-34del	XP_011515255.1:n.867-36_867-34del
XM_011516954.1:c.867-36_867-34del	XP_011515256.1:n.867-36_867-34del
XR_428377.2:n.1479-36_1479-34del
NM_001321961.1:c.1167-36_1167-34del	NP_001308890.1:n.1167-36_1167-34del
NM_001321962.1:c.981-36_981-34del	NP_001308891.1:n.981-36_981-34del
NM_001321963.1:c.867-36_867-34del	NP_001308892.1:n.867-36_867-34del
NM_001321964.1:c.867-36_867-34del	NP_001308893.1:n.867-36_867-34del
NM_001321965.1:c.867-36_867-34del	NP_001308894.1:n.867-36_867-34del
NM_001321966.1:c.807-36_807-34del	NP_001308895.1:n.807-36_807-34del
NM_012472.5:c.1227-36_1227-34del	NP_036604.2:n.1227-36_1227-34del
NR_073525.2:n.1451-36_1451-34del
NR_135905.1:n.1440-36_1440-34del
NR_135906.1:n.881-36_881-34del
NR_135907.1:n.1127-36_1127-34del
NR_135908.1:n.821-36_821-34del
NR_135909.1:n.1245-36_1245-34del
NR_135910.1:n.1552-36_1552-34del
NR_135911.1:n.1631-36_1631-34del
NR_135912.1:n.2190-36_2190-34del
NR_135913.1:n.1877-36_1877-34del
XM_006716538.3:c.1245-36_1245-34del	XP_006716601.2:n.1245-36_1245-34del
XM_011516950.2:c.1185-36_1185-34del	XP_011515252.1:n.1185-36_1185-34del
XM_017013296.1:c.1125-36_1125-34del	XP_016868785.1:n.1125-36_1125-34del
XM_017013297.1:c.867-36_867-34del	XP_016868786.1:n.867-36_867-34del
XM_017013298.1:c.867-36_867-34del	XP_016868787.1:n.867-36_867-34del
NM_012472.6:c.1227-36_1227-34del MANE Select	NP_036604.2:n.1227-36_1227-34del
NM_001321961.2:c.1167-36_1167-34del	NP_001308890.1:n.1167-36_1167-34del
NM_001321962.2:c.981-36_981-34del	NP_001308891.1:n.981-36_981-34del
NM_001321963.2:c.867-36_867-34del	NP_001308892.1:n.867-36_867-34del
NM_001321964.2:c.867-36_867-34del	NP_001308893.1:n.867-36_867-34del
NM_001321965.2:c.867-36_867-34del	NP_001308894.1:n.867-36_867-34del
NM_001321966.2:c.807-36_807-34del	NP_001308895.1:n.807-36_807-34del
NR_073525.3:n.1379-36_1379-34del
NR_135905.2:n.1368-36_1368-34del
NR_135906.2:n.809-36_809-34del
NR_135907.2:n.1055-36_1055-34del
NR_135908.2:n.749-36_749-34del
NR_135909.2:n.1265-36_1265-34del
NR_135910.2:n.1615-36_1615-34del
NR_135911.2:n.1735-36_1735-34del
NR_135912.2:n.2294-36_2294-34del
NR_135913.2:n.1981-36_1981-34del