Canonical Allele Identifier: CA1820845778

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572413_132572415delinsCTA , CM000670.2:g.132572413_132572415delinsCTA	GRCh38
NC_000008.10:g.133584661_133584663delinsCTA , CM000670.1:g.133584661_133584663delinsCTA	GRCh37
NC_000008.9:g.133653843_133653845delinsCTA	NCBI36
NG_033068.1:g.108201_108203delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1292_1294delinsTAG MANE Select	ENSP00000484634.1:p.Ile431=
ENST00000250173.5:c.*156_*158delinsTAG	ENSP00000250173.2:n.*156_*158delinsTAG
ENST00000518642.5:c.*156_*158delinsTAG	ENSP00000428610.1:n.*156_*158delinsTAG
ENST00000519595.5:c.1292_1294delinsTAG	ENSP00000429791.1:p.Ile431=
ENST00000522789.5:c.512_514delinsTAG	ENSP00000428015.1:p.Ile171=
ENST00000618342.1:c.1292_1294delinsTAG	ENSP00000484802.1:p.Ile431=
ENST00000620350.4:c.1292_1294delinsTAG	ENSP00000484634.1:p.Ile431=
NM_012472.4:c.1292_1294delinsTAG	NP_036604.2:p.Ile431=
NR_073525.1:n.1516_1518delinsTAG
XM_006716538.2:c.1310_1312delinsTAG	XP_006716601.2:p.Ile437=
XM_011516950.1:c.1250_1252delinsTAG	XP_011515252.1:p.Ile417=
XM_011516952.1:c.1046_1048delinsTAG	XP_011515254.1:p.Ile349=
XM_011516953.1:c.932_934delinsTAG	XP_011515255.1:p.Ile311=
XM_011516954.1:c.932_934delinsTAG	XP_011515256.1:p.Ile311=
XR_428377.2:n.1544_1546delinsTAG
NM_001321961.1:c.1232_1234delinsTAG	NP_001308890.1:p.Ile411=
NM_001321962.1:c.1046_1048delinsTAG	NP_001308891.1:p.Ile349=
NM_001321963.1:c.932_934delinsTAG	NP_001308892.1:p.Ile311=
NM_001321964.1:c.932_934delinsTAG	NP_001308893.1:p.Ile311=
NM_001321965.1:c.932_934delinsTAG	NP_001308894.1:p.Ile311=
NM_001321966.1:c.872_874delinsTAG	NP_001308895.1:p.Ile291=
NM_012472.5:c.1292_1294delinsTAG	NP_036604.2:p.Ile431=
NR_073525.2:n.1516_1518delinsTAG
NR_135905.1:n.1505_1507delinsTAG
NR_135906.1:n.946_948delinsTAG
NR_135907.1:n.1192_1194delinsTAG
NR_135908.1:n.886_888delinsTAG
NR_135909.1:n.1310_1312delinsTAG
NR_135910.1:n.1617_1619delinsTAG
NR_135911.1:n.1696_1698delinsTAG
NR_135912.1:n.2255_2257delinsTAG
NR_135913.1:n.1942_1944delinsTAG
XM_006716538.3:c.1310_1312delinsTAG	XP_006716601.2:p.Ile437=
XM_011516950.2:c.1250_1252delinsTAG	XP_011515252.1:p.Ile417=
XM_017013296.1:c.1190_1192delinsTAG	XP_016868785.1:p.Ile397=
XM_017013297.1:c.932_934delinsTAG	XP_016868786.1:p.Ile311=
XM_017013298.1:c.932_934delinsTAG	XP_016868787.1:p.Ile311=
NM_012472.6:c.1292_1294delinsTAG MANE Select	NP_036604.2:p.Ile431=
NM_001321961.2:c.1232_1234delinsTAG	NP_001308890.1:p.Ile411=
NM_001321962.2:c.1046_1048delinsTAG	NP_001308891.1:p.Ile349=
NM_001321963.2:c.932_934delinsTAG	NP_001308892.1:p.Ile311=
NM_001321964.2:c.932_934delinsTAG	NP_001308893.1:p.Ile311=
NM_001321965.2:c.932_934delinsTAG	NP_001308894.1:p.Ile311=
NM_001321966.2:c.872_874delinsTAG	NP_001308895.1:p.Ile291=
NR_073525.3:n.1444_1446delinsTAG
NR_135905.2:n.1433_1435delinsTAG
NR_135906.2:n.874_876delinsTAG
NR_135907.2:n.1120_1122delinsTAG
NR_135908.2:n.814_816delinsTAG
NR_135909.2:n.1330_1332delinsTAG
NR_135910.2:n.1680_1682delinsTAG
NR_135911.2:n.1800_1802delinsTAG
NR_135912.2:n.2359_2361delinsTAG
NR_135913.2:n.2046_2048delinsTAG