Canonical Allele Identifier: CA1820870643

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632774_132632775delinsCA , CM000670.2:g.132632774_132632775delinsCA	GRCh38
NC_000008.10:g.133645020_133645021delinsCA , CM000670.1:g.133645020_133645021delinsCA	GRCh37
NC_000008.9:g.133714202_133714203delinsCA	NCBI36
NG_033068.1:g.47843_47844delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000620350.5:c.618_619delinsTG MANE Select	ENSP00000484634.1:p.Phe206=
ENST00000250173.5:c.618_619delinsTG	ENSP00000250173.2:p.Phe206=
ENST00000518642.5:c.618_619delinsTG	ENSP00000428610.1:p.Phe206=
ENST00000519595.5:c.618_619delinsTG	ENSP00000429791.1:p.Phe206=
ENST00000520446.5:n.528+5160_528+5161delinsTG
ENST00000523503.1:n.415+5160_415+5161delinsTG
ENST00000618342.1:c.618_619delinsTG	ENSP00000484802.1:p.Phe206=
ENST00000620350.4:c.618_619delinsTG	ENSP00000484634.1:p.Phe206=
NM_012472.4:c.618_619delinsTG	NP_036604.2:p.Phe206=
NR_073525.1:n.742_743delinsTG
XM_006716538.2:c.636_637delinsTG	XP_006716601.2:p.Phe212=
XM_011516950.1:c.636_637delinsTG	XP_011515252.1:p.Phe212=
XM_011516951.1:c.636_637delinsTG	XP_011515253.1:p.Phe212=
XM_011516952.1:c.372_373delinsTG	XP_011515254.1:p.Phe124=
XM_011516953.1:c.258_259delinsTG	XP_011515255.1:p.Phe86=
XM_011516954.1:c.258_259delinsTG	XP_011515256.1:p.Phe86=
XR_428377.2:n.761_762delinsTG
NM_001321961.1:c.618_619delinsTG	NP_001308890.1:p.Phe206=
NM_001321962.1:c.372_373delinsTG	NP_001308891.1:p.Phe124=
NM_001321963.1:c.258_259delinsTG	NP_001308892.1:p.Phe86=
NM_001321964.1:c.258_259delinsTG	NP_001308893.1:p.Phe86=
NM_001321965.1:c.258_259delinsTG	NP_001308894.1:p.Phe86=
NM_001321966.1:c.258_259delinsTG	NP_001308895.1:p.Phe86=
NM_012472.5:c.618_619delinsTG	NP_036604.2:p.Phe206=
NR_073525.2:n.742_743delinsTG
NR_135905.1:n.866+5160_866+5161delinsTG
NR_135906.1:n.307+5160_307+5161delinsTG
NR_135907.1:n.553+5160_553+5161delinsTG
NR_135908.1:n.307+5160_307+5161delinsTG
NR_135909.1:n.671+5160_671+5161delinsTG
NR_135910.1:n.978+5160_978+5161delinsTG
NR_135911.1:n.1057+5160_1057+5161delinsTG
NR_135912.1:n.1616+5160_1616+5161delinsTG
NR_135913.1:n.1303+5160_1303+5161delinsTG
XM_006716538.3:c.636_637delinsTG	XP_006716601.2:p.Phe212=
XM_011516950.2:c.636_637delinsTG	XP_011515252.1:p.Phe212=
XM_017013296.1:c.516_517delinsTG	XP_016868785.1:p.Phe172=
XM_017013297.1:c.258_259delinsTG	XP_016868786.1:p.Phe86=
XM_017013298.1:c.258_259delinsTG	XP_016868787.1:p.Phe86=
NM_012472.6:c.618_619delinsTG MANE Select	NP_036604.2:p.Phe206=
NM_001321961.2:c.618_619delinsTG	NP_001308890.1:p.Phe206=
NM_001321962.2:c.372_373delinsTG	NP_001308891.1:p.Phe124=
NM_001321963.2:c.258_259delinsTG	NP_001308892.1:p.Phe86=
NM_001321964.2:c.258_259delinsTG	NP_001308893.1:p.Phe86=
NM_001321965.2:c.258_259delinsTG	NP_001308894.1:p.Phe86=
NM_001321966.2:c.258_259delinsTG	NP_001308895.1:p.Phe86=
NR_073525.3:n.670_671delinsTG
NR_135905.2:n.794+5160_794+5161delinsTG
NR_135906.2:n.235+5160_235+5161delinsTG
NR_135907.2:n.481+5160_481+5161delinsTG
NR_135908.2:n.235+5160_235+5161delinsTG
NR_135909.2:n.691+5160_691+5161delinsTG
NR_135910.2:n.1041+5160_1041+5161delinsTG
NR_135911.2:n.1161+5160_1161+5161delinsTG
NR_135912.2:n.1720+5160_1720+5161delinsTG
NR_135913.2:n.1407+5160_1407+5161delinsTG