Canonical Allele Identifier: CA2688631066

Gene: DNAAF11

Linked Data

• gnomAD v4: 8-132572592-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572593_132572594insCTG , CM000670.2:g.132572593_132572594insCTG	GRCh38
NC_000008.10:g.133584841_133584842insCTG , CM000670.1:g.133584841_133584842insCTG	GRCh37
NC_000008.9:g.133654023_133654024insCTG	NCBI36
NG_033068.1:g.108023_108024insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1227-113_1227-112insAGC MANE Select	ENSP00000484634.1:n.1227-113_1227-112insAGC
ENST00000250173.5:c.*91-113_*91-112insAGC	ENSP00000250173.2:n.*91-113_*91-112insAGC
ENST00000518642.5:c.*91-113_*91-112insAGC	ENSP00000428610.1:n.*91-113_*91-112insAGC
ENST00000519595.5:c.1227-113_1227-112insAGC	ENSP00000429791.1:n.1227-113_1227-112insAGC
ENST00000522597.1:n.496-113_496-112insAGC
ENST00000522789.5:c.447-113_447-112insAGC	ENSP00000428015.1:n.447-113_447-112insAGC
ENST00000618342.1:c.1227-113_1227-112insAGC	ENSP00000484802.1:n.1227-113_1227-112insAGC
ENST00000620350.4:c.1227-113_1227-112insAGC	ENSP00000484634.1:n.1227-113_1227-112insAGC
NM_012472.4:c.1227-113_1227-112insAGC	NP_036604.2:n.1227-113_1227-112insAGC
NR_073525.1:n.1451-113_1451-112insAGC
XM_006716538.2:c.1245-113_1245-112insAGC	XP_006716601.2:n.1245-113_1245-112insAGC
XM_011516950.1:c.1185-113_1185-112insAGC	XP_011515252.1:n.1185-113_1185-112insAGC
XM_011516952.1:c.981-113_981-112insAGC	XP_011515254.1:n.981-113_981-112insAGC
XM_011516953.1:c.867-113_867-112insAGC	XP_011515255.1:n.867-113_867-112insAGC
XM_011516954.1:c.867-113_867-112insAGC	XP_011515256.1:n.867-113_867-112insAGC
XR_428377.2:n.1479-113_1479-112insAGC
NM_001321961.1:c.1167-113_1167-112insAGC	NP_001308890.1:n.1167-113_1167-112insAGC
NM_001321962.1:c.981-113_981-112insAGC	NP_001308891.1:n.981-113_981-112insAGC
NM_001321963.1:c.867-113_867-112insAGC	NP_001308892.1:n.867-113_867-112insAGC
NM_001321964.1:c.867-113_867-112insAGC	NP_001308893.1:n.867-113_867-112insAGC
NM_001321965.1:c.867-113_867-112insAGC	NP_001308894.1:n.867-113_867-112insAGC
NM_001321966.1:c.807-113_807-112insAGC	NP_001308895.1:n.807-113_807-112insAGC
NM_012472.5:c.1227-113_1227-112insAGC	NP_036604.2:n.1227-113_1227-112insAGC
NR_073525.2:n.1451-113_1451-112insAGC
NR_135905.1:n.1440-113_1440-112insAGC
NR_135906.1:n.881-113_881-112insAGC
NR_135907.1:n.1127-113_1127-112insAGC
NR_135908.1:n.821-113_821-112insAGC
NR_135909.1:n.1245-113_1245-112insAGC
NR_135910.1:n.1552-113_1552-112insAGC
NR_135911.1:n.1631-113_1631-112insAGC
NR_135912.1:n.2190-113_2190-112insAGC
NR_135913.1:n.1877-113_1877-112insAGC
XM_006716538.3:c.1245-113_1245-112insAGC	XP_006716601.2:n.1245-113_1245-112insAGC
XM_011516950.2:c.1185-113_1185-112insAGC	XP_011515252.1:n.1185-113_1185-112insAGC
XM_017013296.1:c.1125-113_1125-112insAGC	XP_016868785.1:n.1125-113_1125-112insAGC
XM_017013297.1:c.867-113_867-112insAGC	XP_016868786.1:n.867-113_867-112insAGC
XM_017013298.1:c.867-113_867-112insAGC	XP_016868787.1:n.867-113_867-112insAGC
NM_012472.6:c.1227-113_1227-112insAGC MANE Select	NP_036604.2:n.1227-113_1227-112insAGC
NM_001321961.2:c.1167-113_1167-112insAGC	NP_001308890.1:n.1167-113_1167-112insAGC
NM_001321962.2:c.981-113_981-112insAGC	NP_001308891.1:n.981-113_981-112insAGC
NM_001321963.2:c.867-113_867-112insAGC	NP_001308892.1:n.867-113_867-112insAGC
NM_001321964.2:c.867-113_867-112insAGC	NP_001308893.1:n.867-113_867-112insAGC
NM_001321965.2:c.867-113_867-112insAGC	NP_001308894.1:n.867-113_867-112insAGC
NM_001321966.2:c.807-113_807-112insAGC	NP_001308895.1:n.807-113_807-112insAGC
NR_073525.3:n.1379-113_1379-112insAGC
NR_135905.2:n.1368-113_1368-112insAGC
NR_135906.2:n.809-113_809-112insAGC
NR_135907.2:n.1055-113_1055-112insAGC
NR_135908.2:n.749-113_749-112insAGC
NR_135909.2:n.1265-113_1265-112insAGC
NR_135910.2:n.1615-113_1615-112insAGC
NR_135911.2:n.1735-113_1735-112insAGC
NR_135912.2:n.2294-113_2294-112insAGC
NR_135913.2:n.1981-113_1981-112insAGC