Canonical Allele Identifier: CA2782264647

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572510_132572511insGACC , CM000670.2:g.132572510_132572511insGACC	GRCh38
NC_000008.10:g.133584758_133584759insGACC , CM000670.1:g.133584758_133584759insGACC	GRCh37
NC_000008.9:g.133653940_133653941insGACC	NCBI36
NG_033068.1:g.108106_108107insGTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1227-30_1227-29insGTCG MANE Select	ENSP00000484634.1:n.1227-30_1227-29insGTCG
ENST00000250173.5:c.*91-30_*91-29insGTCG	ENSP00000250173.2:n.*91-30_*91-29insGTCG
ENST00000518642.5:c.*91-30_*91-29insGTCG	ENSP00000428610.1:n.*91-30_*91-29insGTCG
ENST00000519595.5:c.1227-30_1227-29insGTCG	ENSP00000429791.1:n.1227-30_1227-29insGTCG
ENST00000522597.1:n.496-30_496-29insGTCG
ENST00000522789.5:c.447-30_447-29insGTCG	ENSP00000428015.1:n.447-30_447-29insGTCG
ENST00000618342.1:c.1227-30_1227-29insGTCG	ENSP00000484802.1:n.1227-30_1227-29insGTCG
ENST00000620350.4:c.1227-30_1227-29insGTCG	ENSP00000484634.1:n.1227-30_1227-29insGTCG
NM_012472.4:c.1227-30_1227-29insGTCG	NP_036604.2:n.1227-30_1227-29insGTCG
NR_073525.1:n.1451-30_1451-29insGTCG
XM_006716538.2:c.1245-30_1245-29insGTCG	XP_006716601.2:n.1245-30_1245-29insGTCG
XM_011516950.1:c.1185-30_1185-29insGTCG	XP_011515252.1:n.1185-30_1185-29insGTCG
XM_011516952.1:c.981-30_981-29insGTCG	XP_011515254.1:n.981-30_981-29insGTCG
XM_011516953.1:c.867-30_867-29insGTCG	XP_011515255.1:n.867-30_867-29insGTCG
XM_011516954.1:c.867-30_867-29insGTCG	XP_011515256.1:n.867-30_867-29insGTCG
XR_428377.2:n.1479-30_1479-29insGTCG
NM_001321961.1:c.1167-30_1167-29insGTCG	NP_001308890.1:n.1167-30_1167-29insGTCG
NM_001321962.1:c.981-30_981-29insGTCG	NP_001308891.1:n.981-30_981-29insGTCG
NM_001321963.1:c.867-30_867-29insGTCG	NP_001308892.1:n.867-30_867-29insGTCG
NM_001321964.1:c.867-30_867-29insGTCG	NP_001308893.1:n.867-30_867-29insGTCG
NM_001321965.1:c.867-30_867-29insGTCG	NP_001308894.1:n.867-30_867-29insGTCG
NM_001321966.1:c.807-30_807-29insGTCG	NP_001308895.1:n.807-30_807-29insGTCG
NM_012472.5:c.1227-30_1227-29insGTCG	NP_036604.2:n.1227-30_1227-29insGTCG
NR_073525.2:n.1451-30_1451-29insGTCG
NR_135905.1:n.1440-30_1440-29insGTCG
NR_135906.1:n.881-30_881-29insGTCG
NR_135907.1:n.1127-30_1127-29insGTCG
NR_135908.1:n.821-30_821-29insGTCG
NR_135909.1:n.1245-30_1245-29insGTCG
NR_135910.1:n.1552-30_1552-29insGTCG
NR_135911.1:n.1631-30_1631-29insGTCG
NR_135912.1:n.2190-30_2190-29insGTCG
NR_135913.1:n.1877-30_1877-29insGTCG
XM_006716538.3:c.1245-30_1245-29insGTCG	XP_006716601.2:n.1245-30_1245-29insGTCG
XM_011516950.2:c.1185-30_1185-29insGTCG	XP_011515252.1:n.1185-30_1185-29insGTCG
XM_017013296.1:c.1125-30_1125-29insGTCG	XP_016868785.1:n.1125-30_1125-29insGTCG
XM_017013297.1:c.867-30_867-29insGTCG	XP_016868786.1:n.867-30_867-29insGTCG
XM_017013298.1:c.867-30_867-29insGTCG	XP_016868787.1:n.867-30_867-29insGTCG
NM_012472.6:c.1227-30_1227-29insGTCG MANE Select	NP_036604.2:n.1227-30_1227-29insGTCG
NM_001321961.2:c.1167-30_1167-29insGTCG	NP_001308890.1:n.1167-30_1167-29insGTCG
NM_001321962.2:c.981-30_981-29insGTCG	NP_001308891.1:n.981-30_981-29insGTCG
NM_001321963.2:c.867-30_867-29insGTCG	NP_001308892.1:n.867-30_867-29insGTCG
NM_001321964.2:c.867-30_867-29insGTCG	NP_001308893.1:n.867-30_867-29insGTCG
NM_001321965.2:c.867-30_867-29insGTCG	NP_001308894.1:n.867-30_867-29insGTCG
NM_001321966.2:c.807-30_807-29insGTCG	NP_001308895.1:n.807-30_807-29insGTCG
NR_073525.3:n.1379-30_1379-29insGTCG
NR_135905.2:n.1368-30_1368-29insGTCG
NR_135906.2:n.809-30_809-29insGTCG
NR_135907.2:n.1055-30_1055-29insGTCG
NR_135908.2:n.749-30_749-29insGTCG
NR_135909.2:n.1265-30_1265-29insGTCG
NR_135910.2:n.1615-30_1615-29insGTCG
NR_135911.2:n.1735-30_1735-29insGTCG
NR_135912.2:n.2294-30_2294-29insGTCG
NR_135913.2:n.1981-30_1981-29insGTCG