Canonical Allele Identifier: CA1820845802

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572468_132572471delinsCATG , CM000670.2:g.132572468_132572471delinsCATG	GRCh38
NC_000008.10:g.133584716_133584719delinsCATG , CM000670.1:g.133584716_133584719delinsCATG	GRCh37
NC_000008.9:g.133653898_133653901delinsCATG	NCBI36
NG_033068.1:g.108145_108148delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1236_1239delinsCATG MANE Select	ENSP00000484634.1:p.His412=
ENST00000250173.5:c.*100_*103delinsCATG	ENSP00000250173.2:n.*100_*103delinsCATG
ENST00000518642.5:c.*100_*103delinsCATG	ENSP00000428610.1:n.*100_*103delinsCATG
ENST00000519595.5:c.1236_1239delinsCATG	ENSP00000429791.1:p.His412=
ENST00000522597.1:n.505_508delinsCATG
ENST00000522789.5:c.456_459delinsCATG	ENSP00000428015.1:p.His152=
ENST00000618342.1:c.1236_1239delinsCATG	ENSP00000484802.1:p.His412=
ENST00000620350.4:c.1236_1239delinsCATG	ENSP00000484634.1:p.His412=
NM_012472.4:c.1236_1239delinsCATG	NP_036604.2:p.His412=
NR_073525.1:n.1460_1463delinsCATG
XM_006716538.2:c.1254_1257delinsCATG	XP_006716601.2:p.His418=
XM_011516950.1:c.1194_1197delinsCATG	XP_011515252.1:p.His398=
XM_011516952.1:c.990_993delinsCATG	XP_011515254.1:p.His330=
XM_011516953.1:c.876_879delinsCATG	XP_011515255.1:p.His292=
XM_011516954.1:c.876_879delinsCATG	XP_011515256.1:p.His292=
XR_428377.2:n.1488_1491delinsCATG
NM_001321961.1:c.1176_1179delinsCATG	NP_001308890.1:p.His392=
NM_001321962.1:c.990_993delinsCATG	NP_001308891.1:p.His330=
NM_001321963.1:c.876_879delinsCATG	NP_001308892.1:p.His292=
NM_001321964.1:c.876_879delinsCATG	NP_001308893.1:p.His292=
NM_001321965.1:c.876_879delinsCATG	NP_001308894.1:p.His292=
NM_001321966.1:c.816_819delinsCATG	NP_001308895.1:p.His272=
NM_012472.5:c.1236_1239delinsCATG	NP_036604.2:p.His412=
NR_073525.2:n.1460_1463delinsCATG
NR_135905.1:n.1449_1452delinsCATG
NR_135906.1:n.890_893delinsCATG
NR_135907.1:n.1136_1139delinsCATG
NR_135908.1:n.830_833delinsCATG
NR_135909.1:n.1254_1257delinsCATG
NR_135910.1:n.1561_1564delinsCATG
NR_135911.1:n.1640_1643delinsCATG
NR_135912.1:n.2199_2202delinsCATG
NR_135913.1:n.1886_1889delinsCATG
XM_006716538.3:c.1254_1257delinsCATG	XP_006716601.2:p.His418=
XM_011516950.2:c.1194_1197delinsCATG	XP_011515252.1:p.His398=
XM_017013296.1:c.1134_1137delinsCATG	XP_016868785.1:p.His378=
XM_017013297.1:c.876_879delinsCATG	XP_016868786.1:p.His292=
XM_017013298.1:c.876_879delinsCATG	XP_016868787.1:p.His292=
NM_012472.6:c.1236_1239delinsCATG MANE Select	NP_036604.2:p.His412=
NM_001321961.2:c.1176_1179delinsCATG	NP_001308890.1:p.His392=
NM_001321962.2:c.990_993delinsCATG	NP_001308891.1:p.His330=
NM_001321963.2:c.876_879delinsCATG	NP_001308892.1:p.His292=
NM_001321964.2:c.876_879delinsCATG	NP_001308893.1:p.His292=
NM_001321965.2:c.876_879delinsCATG	NP_001308894.1:p.His292=
NM_001321966.2:c.816_819delinsCATG	NP_001308895.1:p.His272=
NR_073525.3:n.1388_1391delinsCATG
NR_135905.2:n.1377_1380delinsCATG
NR_135906.2:n.818_821delinsCATG
NR_135907.2:n.1064_1067delinsCATG
NR_135908.2:n.758_761delinsCATG
NR_135909.2:n.1274_1277delinsCATG
NR_135910.2:n.1624_1627delinsCATG
NR_135911.2:n.1744_1747delinsCATG
NR_135912.2:n.2303_2306delinsCATG
NR_135913.2:n.1990_1993delinsCATG