Canonical Allele Identifier: CA4881098

Gene: DNAAF11

Linked Data

• dbSNP Id: rs759171476
• ExAC: 8:133584738 C / CAAA
• gnomAD v2: 8-133584738-C-CAAA
• gnomAD v4: 8-132572490-C-CAAA
• MyVariant Identifiers: chr8:g.133584738_133584739insAAA (hg19) ; chr8:g.132572490_132572491insAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572495_132572497dup , CM000670.2:g.132572495_132572497dup	GRCh38
NC_000008.10:g.133584743_133584745dup , CM000670.1:g.133584743_133584745dup	GRCh37
NC_000008.9:g.133653925_133653927dup	NCBI36
NG_033068.1:g.108123_108125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1227-13_1227-11dup MANE Select	ENSP00000484634.1:n.1227-13_1227-11dup
ENST00000250173.5:c.*91-13_*91-11dup	ENSP00000250173.2:n.*91-13_*91-11dup
ENST00000518642.5:c.*91-13_*91-11dup	ENSP00000428610.1:n.*91-13_*91-11dup
ENST00000519595.5:c.1227-13_1227-11dup	ENSP00000429791.1:n.1227-13_1227-11dup
ENST00000522597.1:n.496-13_496-11dup
ENST00000522789.5:c.447-13_447-11dup	ENSP00000428015.1:n.447-13_447-11dup
ENST00000618342.1:c.1227-13_1227-11dup	ENSP00000484802.1:n.1227-13_1227-11dup
ENST00000620350.4:c.1227-13_1227-11dup	ENSP00000484634.1:n.1227-13_1227-11dup
NM_012472.4:c.1227-13_1227-11dup	NP_036604.2:n.1227-13_1227-11dup
NR_073525.1:n.1451-13_1451-11dup
XM_006716538.2:c.1245-13_1245-11dup	XP_006716601.2:n.1245-13_1245-11dup
XM_011516950.1:c.1185-13_1185-11dup	XP_011515252.1:n.1185-13_1185-11dup
XM_011516952.1:c.981-13_981-11dup	XP_011515254.1:n.981-13_981-11dup
XM_011516953.1:c.867-13_867-11dup	XP_011515255.1:n.867-13_867-11dup
XM_011516954.1:c.867-13_867-11dup	XP_011515256.1:n.867-13_867-11dup
XR_428377.2:n.1479-13_1479-11dup
NM_001321961.1:c.1167-13_1167-11dup	NP_001308890.1:n.1167-13_1167-11dup
NM_001321962.1:c.981-13_981-11dup	NP_001308891.1:n.981-13_981-11dup
NM_001321963.1:c.867-13_867-11dup	NP_001308892.1:n.867-13_867-11dup
NM_001321964.1:c.867-13_867-11dup	NP_001308893.1:n.867-13_867-11dup
NM_001321965.1:c.867-13_867-11dup	NP_001308894.1:n.867-13_867-11dup
NM_001321966.1:c.807-13_807-11dup	NP_001308895.1:n.807-13_807-11dup
NM_012472.5:c.1227-13_1227-11dup	NP_036604.2:n.1227-13_1227-11dup
NR_073525.2:n.1451-13_1451-11dup
NR_135905.1:n.1440-13_1440-11dup
NR_135906.1:n.881-13_881-11dup
NR_135907.1:n.1127-13_1127-11dup
NR_135908.1:n.821-13_821-11dup
NR_135909.1:n.1245-13_1245-11dup
NR_135910.1:n.1552-13_1552-11dup
NR_135911.1:n.1631-13_1631-11dup
NR_135912.1:n.2190-13_2190-11dup
NR_135913.1:n.1877-13_1877-11dup
XM_006716538.3:c.1245-13_1245-11dup	XP_006716601.2:n.1245-13_1245-11dup
XM_011516950.2:c.1185-13_1185-11dup	XP_011515252.1:n.1185-13_1185-11dup
XM_017013296.1:c.1125-13_1125-11dup	XP_016868785.1:n.1125-13_1125-11dup
XM_017013297.1:c.867-13_867-11dup	XP_016868786.1:n.867-13_867-11dup
XM_017013298.1:c.867-13_867-11dup	XP_016868787.1:n.867-13_867-11dup
NM_012472.6:c.1227-13_1227-11dup MANE Select	NP_036604.2:n.1227-13_1227-11dup
NM_001321961.2:c.1167-13_1167-11dup	NP_001308890.1:n.1167-13_1167-11dup
NM_001321962.2:c.981-13_981-11dup	NP_001308891.1:n.981-13_981-11dup
NM_001321963.2:c.867-13_867-11dup	NP_001308892.1:n.867-13_867-11dup
NM_001321964.2:c.867-13_867-11dup	NP_001308893.1:n.867-13_867-11dup
NM_001321965.2:c.867-13_867-11dup	NP_001308894.1:n.867-13_867-11dup
NM_001321966.2:c.807-13_807-11dup	NP_001308895.1:n.807-13_807-11dup
NR_073525.3:n.1379-13_1379-11dup
NR_135905.2:n.1368-13_1368-11dup
NR_135906.2:n.809-13_809-11dup
NR_135907.2:n.1055-13_1055-11dup
NR_135908.2:n.749-13_749-11dup
NR_135909.2:n.1265-13_1265-11dup
NR_135910.2:n.1615-13_1615-11dup
NR_135911.2:n.1735-13_1735-11dup
NR_135912.2:n.2294-13_2294-11dup
NR_135913.2:n.1981-13_1981-11dup